Canonical Allele Identifier: CA1468148819

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404577_73404578delinsAT , CM000666.2:g.73404577_73404578delinsAT	GRCh38
NC_000004.11:g.74270294_74270295delinsAT , CM000666.1:g.74270294_74270295delinsAT	GRCh37
NC_000004.10:g.74489158_74489159delinsAT	NCBI36
NG_009291.1:g.5323_5324delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.79+171_79+172delinsAT MANE Select	ENSP00000295897.4:n.79+171_79+172delinsAT
ENST00000295897.8:c.79+171_79+172delinsAT	ENSP00000295897.4:n.79+171_79+172delinsAT
ENST00000401494.7:c.79+171_79+172delinsAT	ENSP00000384695.3:n.79+171_79+172delinsAT
ENST00000415165.6:c.79+171_79+172delinsAT	ENSP00000401820.2:n.79+171_79+172delinsAT
ENST00000441319.5:c.85+171_85+172delinsAT	ENSP00000392541.1:n.85+171_85+172delinsAT
ENST00000476441.6:c.79+171_79+172delinsAT	ENSP00000423727.1:n.79+171_79+172delinsAT
ENST00000503124.5:c.-102+171_-102+172delinsAT	ENSP00000421027.1:n.-102+171_-102+172delinsAT
ENST00000509063.5:c.79+171_79+172delinsAT	ENSP00000422784.1:n.79+171_79+172delinsAT
ENST00000510166.5:n.120+171_120+172delinsAT
ENST00000514786.1:n.48+241_48+242delinsAT
ENST00000515133.5:n.120+171_120+172delinsAT
ENST00000621085.4:c.79+171_79+172delinsAT	ENSP00000483421.1:n.79+171_79+172delinsAT
ENST00000621628.4:c.79+171_79+172delinsAT	ENSP00000480485.1:n.79+171_79+172delinsAT
NM_000477.5:c.79+171_79+172delinsAT	NP_000468.1:n.79+171_79+172delinsAT
NM_000477.6:c.79+171_79+172delinsAT	NP_000468.1:n.79+171_79+172delinsAT
NM_000477.7:c.79+171_79+172delinsAT MANE Select	NP_000468.1:n.79+171_79+172delinsAT