Canonical Allele Identifier: CA357241596

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280876G>T (hg19) ; chr4:g.73415159G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415159G>T , CM000666.2:g.73415159G>T	GRCh38
NC_000004.11:g.74280876G>T , CM000666.1:g.74280876G>T	GRCh37
NC_000004.10:g.74499740G>T	NCBI36
NG_009291.1:g.15905G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1183G>T MANE Select	ENSP00000295897.4:p.Ala395Ser
ENST00000295897.8:c.1183G>T	ENSP00000295897.4:p.Ala395Ser
ENST00000401494.7:c.838G>T	ENSP00000384695.3:p.Ala280Ser
ENST00000415165.6:c.607G>T	ENSP00000401820.2:p.Ala203Ser
ENST00000476441.6:c.*462G>T	ENSP00000423727.1:n.*462G>T
ENST00000484992.1:n.503G>T
ENST00000503124.5:c.733G>T	ENSP00000421027.1:p.Ala245Ser
ENST00000504043.1:n.186G>T
ENST00000505649.5:n.869G>T
ENST00000509063.5:c.1183G>T	ENSP00000422784.1:p.Ala395Ser
ENST00000511370.1:c.716G>T
ENST00000621085.4:c.544G>T	ENSP00000483421.1:p.Ala182Ser
ENST00000621628.4:c.544G>T	ENSP00000480485.1:p.Ala182Ser
NM_000477.5:c.1183G>T	NP_000468.1:p.Ala395Ser
NM_000477.6:c.1183G>T	NP_000468.1:p.Ala395Ser
NM_000477.7:c.1183G>T MANE Select	NP_000468.1:p.Ala395Ser