Canonical Allele Identifier: CA2207428182

Gene: CLEC16A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11098570_11098571delinsAC , CM000678.2:g.11098570_11098571delinsAC	GRCh38
NC_000016.9:g.11192427_11192428delinsAC , CM000678.1:g.11192427_11192428delinsAC	GRCh37
NC_000016.8:g.11099928_11099929delinsAC	NCBI36
NG_016757.1:g.159083_159084delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000703130.1:c.2111-22045_2111-22044delinsAC	ENSP00000515187.1:n.2111-22045_2111-22044...
ENST00000409790.6:c.2117-22045_2117-22044delinsAC MANE Select	ENSP00000387122.1:n.2117-22045_2117-22044...
ENST00000646363.1:n.778-22045_778-22044delinsAC
ENST00000409552.4:c.2063-22045_2063-22044delinsAC	ENSP00000386495.3:n.2063-22045_2063-22044...
ENST00000409790.5:c.2117-22045_2117-22044delinsAC	ENSP00000387122.1:n.2117-22045_2117-22044...
ENST00000465491.5:n.773-22045_773-22044delinsAC
NM_001243403.1:c.2063-22045_2063-22044delinsAC	NP_001230332.1:n.2063-22045_2063-22044del...
NM_015226.2:c.2117-22045_2117-22044delinsAC	NP_056041.1:n.2117-22045_2117-22044delins...
XM_005255210.1:c.2111-22045_2111-22044delinsAC	XP_005255267.1:n.2111-22045_2111-22044del...
XM_005255211.1:c.2069-22045_2069-22044delinsAC	XP_005255268.1:n.2069-22045_2069-22044del...
XM_005255213.1:c.2063-22045_2063-22044delinsAC	XP_005255270.1:n.2063-22045_2063-22044del...
XM_005255214.1:c.2117-22045_2117-22044delinsAC	XP_005255271.1:n.2117-22045_2117-22044del...
XM_005255215.3:c.2117-22045_2117-22044delinsAC	XP_005255272.1:n.2117-22045_2117-22044del...
XM_005255216.1:c.2117-22045_2117-22044delinsAC	XP_005255273.1:n.2117-22045_2117-22044del...
XM_011522434.1:c.1988-22045_1988-22044delinsAC	XP_011520736.1:n.1988-22045_1988-22044del...
XM_011522435.1:c.2117-22045_2117-22044delinsAC	XP_011520737.1:n.2117-22045_2117-22044del...
XM_011522436.1:c.2117-22045_2117-22044delinsAC	XP_011520738.1:n.2117-22045_2117-22044del...
XM_011522437.1:c.2117-22045_2117-22044delinsAC	XP_011520739.1:n.2117-22045_2117-22044del...
XM_011522438.1:c.2117-22045_2117-22044delinsAC	XP_011520740.1:n.2117-22045_2117-22044del...
XM_011522439.1:c.2117-22045_2117-22044delinsAC	XP_011520741.1:n.2117-22045_2117-22044del...
XM_011522440.1:c.2117-22045_2117-22044delinsAC	XP_011520742.1:n.2117-22045_2117-22044del...
XR_932810.1:n.2341-22045_2341-22044delinsAC
XM_005255210.2:c.2111-22045_2111-22044delinsAC	XP_005255267.1:n.2111-22045_2111-22044del...
XM_005255211.2:c.2069-22045_2069-22044delinsAC	XP_005255268.1:n.2069-22045_2069-22044del...
XM_005255213.2:c.2063-22045_2063-22044delinsAC	XP_005255270.1:n.2063-22045_2063-22044del...
XM_005255214.2:c.2117-22045_2117-22044delinsAC	XP_005255271.1:n.2117-22045_2117-22044del...
XM_005255215.4:c.2117-22045_2117-22044delinsAC	XP_005255272.1:n.2117-22045_2117-22044del...
XM_005255216.2:c.2117-22045_2117-22044delinsAC	XP_005255273.1:n.2117-22045_2117-22044del...
XM_011522434.2:c.1988-22045_1988-22044delinsAC	XP_011520736.1:n.1988-22045_1988-22044del...
XM_011522435.2:c.2117-22045_2117-22044delinsAC	XP_011520737.1:n.2117-22045_2117-22044del...
XM_011522436.3:c.2117-22045_2117-22044delinsAC	XP_011520738.1:n.2117-22045_2117-22044del...
XM_011522437.3:c.2117-22045_2117-22044delinsAC	XP_011520739.1:n.2117-22045_2117-22044del...
XM_011522438.3:c.2117-22045_2117-22044delinsAC	XP_011520740.1:n.2117-22045_2117-22044del...
XM_011522439.3:c.2117-22045_2117-22044delinsAC	XP_011520741.1:n.2117-22045_2117-22044del...
XM_011522440.3:c.2117-22045_2117-22044delinsAC	XP_011520742.1:n.2117-22045_2117-22044del...
XM_017023090.2:c.602-22045_602-22044delinsAC	XP_016878579.1:n.602-22045_602-22044delin...
XM_024450218.1:c.2069-22045_2069-22044delinsAC	XP_024305986.1:n.2069-22045_2069-22044del...
XM_024450219.1:c.668-22045_668-22044delinsAC	XP_024305987.1:n.668-22045_668-22044delin...
XR_932810.3:n.2296-22045_2296-22044delinsAC
NM_015226.3:c.2117-22045_2117-22044delinsAC MANE Select	NP_056041.1:n.2117-22045_2117-22044delins...
NM_001243403.2:c.2063-22045_2063-22044delinsAC	NP_001230332.1:n.2063-22045_2063-22044del...