Canonical Allele Identifier: CA1468146818

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418139A= , CM000666.2:g.73418139A=	GRCh38
NC_000004.11:g.74283856A= , CM000666.1:g.74283856A=	GRCh37
NC_000004.10:g.74502720A=	NCBI36
NG_009291.1:g.18885A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1480A= MANE Select	ENSP00000295897.4:p.Ser494=
ENST00000295897.8:c.1480A=	ENSP00000295897.4:p.Ser494=
ENST00000401494.7:c.1135A=	ENSP00000384695.3:p.Ser379=
ENST00000415165.6:c.904A=	ENSP00000401820.2:p.Ser302=
ENST00000476441.6:c.*759A=	ENSP00000423727.1:n.*759A=
ENST00000486939.1:n.134A=
ENST00000503124.5:c.1030A=	ENSP00000421027.1:p.Ser344=
ENST00000505649.5:n.1027A=
ENST00000509063.5:c.1480A=	ENSP00000422784.1:p.Ser494=
ENST00000511370.1:c.1013A=
ENST00000621085.4:c.841A=	ENSP00000483421.1:p.Ser281=
ENST00000621628.4:c.841A=	ENSP00000480485.1:p.Ser281=
NM_000477.5:c.1480A=	NP_000468.1:p.Ser494=
NM_000477.6:c.1480A=	NP_000468.1:p.Ser494=
NM_000477.7:c.1480A= MANE Select	NP_000468.1:p.Ser494=