Canonical Allele Identifier: CA2207457622

Gene: CLEC16A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11150801G= , CM000678.2:g.11150801G=	GRCh38
NC_000016.9:g.11244658G= , CM000678.1:g.11244658G=	GRCh37
NC_000016.8:g.11152159G=	NCBI36
NG_016757.1:g.211314G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015226.3:c.2642-15587G= MANE Select	NP_056041.1:n.2642-15587G=
ENST00000409790.6:c.2642-15587G= MANE Select	ENSP00000387122.1:n.2642-15587G=
NM_015226.2:c.2642-15587G=	NP_056041.1:n.2642-15587G=
ENST00000261657.5:c.216-15587G=
ENST00000409790.5:c.2642-15587G=	ENSP00000387122.1:n.2642-15587G=
ENST00000428742.6:c.373-6276G=
ENST00000436973.5:c.221-5773G=	ENSP00000389963.1:n.221-5773G=
ENST00000703130.1:c.2636-15587G=	ENSP00000515187.1:n.2636-15587G=
XM_005255210.1:c.2636-15587G=	XP_005255267.1:n.2636-15587G=
XM_005255210.2:c.2636-15587G=	XP_005255267.1:n.2636-15587G=
XM_005255211.1:c.2594-15587G=	XP_005255268.1:n.2594-15587G=
XM_005255211.2:c.2594-15587G=	XP_005255268.1:n.2594-15587G=
XM_005255213.1:c.2588-15587G=	XP_005255270.1:n.2588-15587G=
XM_005255213.2:c.2588-15587G=	XP_005255270.1:n.2588-15587G=
XM_005255214.1:c.2641+24655G=	XP_005255271.1:n.2641+24655G=
XM_005255214.2:c.2641+24655G=	XP_005255271.1:n.2641+24655G=
XM_005255215.3:c.2642-5773G=	XP_005255272.1:n.2642-5773G=
XM_005255215.4:c.2642-5773G=	XP_005255272.1:n.2642-5773G=
XM_005255216.1:c.2642-6276G=	XP_005255273.1:n.2642-6276G=
XM_005255216.2:c.2642-6276G=	XP_005255273.1:n.2642-6276G=
XM_011522434.1:c.2513-15587G=	XP_011520736.1:n.2513-15587G=
XM_011522434.2:c.2513-15587G=	XP_011520736.1:n.2513-15587G=
XM_011522435.1:c.2642-15587G=	XP_011520737.1:n.2642-15587G=
XM_011522435.2:c.2642-15587G=	XP_011520737.1:n.2642-15587G=
XM_011522438.3:c.*872G=	XP_011520740.1:n.*872G=
XM_017023090.2:c.1127-15587G=	XP_016878579.1:n.1127-15587G=
XM_024450218.1:c.2594-5773G=	XP_024305986.1:n.2594-5773G=
XM_024450219.1:c.1193-15587G=	XP_024305987.1:n.1193-15587G=
XR_932810.1:n.2866-15587G=
XR_932810.3:n.2821-15587G=