Canonical Allele Identifier: CA224144403

Gene: CABP4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67458294_67458298del , CM000673.2:g.67458294_67458298del	GRCh38
NC_000011.9:g.67225765_67225769del , CM000673.1:g.67225765_67225769del	GRCh37
NC_000011.8:g.66982341_66982345del	NCBI36
NG_021211.1:g.7948_7952del

Transcript Alleles

HGVS	Amino-acid Change
NM_145200.5:c.652-77_652-73del MANE Select	NP_660201.1:n.652-77_652-73del
ENST00000325656.7:c.652-77_652-73del MANE Select	ENSP00000324960.5:n.652-77_652-73del
NM_001300895.1:c.337-77_337-73del	NP_001287824.1:n.337-77_337-73del
NM_001300895.2:c.337-77_337-73del	NP_001287824.1:n.337-77_337-73del
NM_001300895.3:c.337-77_337-73del	NP_001287824.1:n.337-77_337-73del
NM_001300896.1:c.337-77_337-73del	NP_001287825.1:n.337-77_337-73del
NM_001300896.2:c.337-77_337-73del	NP_001287825.1:n.337-77_337-73del
NM_001300896.3:c.337-77_337-73del	NP_001287825.1:n.337-77_337-73del
NM_001379183.1:c.337-77_337-73del	NP_001366112.1:n.337-77_337-73del
NM_145200.3:c.652-77_652-73del	NP_660201.1:n.652-77_652-73del
NM_145200.4:c.652-77_652-73del	NP_660201.1:n.652-77_652-73del
NR_166529.1:n.547-77_547-73del
ENST00000325656.6:c.652-77_652-73del	ENSP00000324960.5:n.652-77_652-73del
ENST00000438189.6:c.337-77_337-73del	ENSP00000401555.2:n.337-77_337-73del
XM_011545181.1:c.712-77_712-73del	XP_011543483.1:n.712-77_712-73del
XM_011545181.2:c.712-77_712-73del	XP_011543483.1:n.712-77_712-73del
XM_011545182.1:c.568-77_568-73del	XP_011543484.1:n.568-77_568-73del
XM_011545182.2:c.568-77_568-73del	XP_011543484.1:n.568-77_568-73del
XM_011545183.1:c.337-77_337-73del	XP_011543485.1:n.337-77_337-73del
XM_011545183.2:c.337-77_337-73del	XP_011543485.1:n.337-77_337-73del
XM_011545184.1:c.337-77_337-73del	XP_011543486.1:n.337-77_337-73del
XM_017018025.1:c.337-77_337-73del	XP_016873514.1:n.337-77_337-73del
XM_024448615.1:c.652-77_652-73del	XP_024304383.1:n.652-77_652-73del
XM_024448616.1:c.337-77_337-73del	XP_024304384.1:n.337-77_337-73del