Canonical Allele Identifier: CA439800261

Gene: ALB

Linked Data

• gnomAD v4: 4-73415053-A-C
• MyVariant Identifiers: chr4:g.74280770A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415053A>C , CM000666.2:g.73415053A>C	GRCh38
NC_000004.11:g.74280770A>C , CM000666.1:g.74280770A>C	GRCh37
NC_000004.10:g.74499634A>C	NCBI36
NG_009291.1:g.15799A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1077A>C MANE Select	ENSP00000295897.4:p.Ala359=
ENST00000295897.8:c.1077A>C	ENSP00000295897.4:p.Ala359=
ENST00000401494.7:c.732A>C	ENSP00000384695.3:p.Ala244=
ENST00000415165.6:c.501A>C	ENSP00000401820.2:p.Ala167=
ENST00000476441.6:c.*356A>C	ENSP00000423727.1:n.*356A>C
ENST00000484992.1:n.397A>C
ENST00000503124.5:c.627A>C	ENSP00000421027.1:p.Ala209=
ENST00000504043.1:n.80A>C
ENST00000505649.5:n.763A>C
ENST00000509063.5:c.1077A>C	ENSP00000422784.1:p.Ala359=
ENST00000511370.1:c.610A>C
ENST00000621085.4:c.491-53A>C	ENSP00000483421.1:n.491-53A>C
ENST00000621628.4:c.487-49A>C	ENSP00000480485.1:n.487-49A>C
NM_000477.5:c.1077A>C	NP_000468.1:p.Ala359=
NM_000477.6:c.1077A>C	NP_000468.1:p.Ala359=
NM_000477.7:c.1077A>C MANE Select	NP_000468.1:p.Ala359=