Canonical Allele Identifier: CA357246278

Gene: ALB

Linked Data

• gnomAD v4: 4-73419562-G-T
• MyVariant Identifiers: chr4:g.74285279G>T (hg19) ; chr4:g.73419562G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419562G>T , CM000666.2:g.73419562G>T	GRCh38
NC_000004.11:g.74285279G>T , CM000666.1:g.74285279G>T	GRCh37
NC_000004.10:g.74504143G>T	NCBI36
NG_009291.1:g.20308G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1708G>T MANE Select	ENSP00000295897.4:p.Ala570Ser
ENST00000295897.8:c.1708G>T	ENSP00000295897.4:p.Ala570Ser
ENST00000401494.7:c.1363G>T	ENSP00000384695.3:p.Ala455Ser
ENST00000415165.6:c.1132G>T	ENSP00000401820.2:p.Ala378Ser
ENST00000476441.6:c.*987G>T	ENSP00000423727.1:n.*987G>T
ENST00000495173.1:n.16G>T
ENST00000503124.5:c.1258G>T	ENSP00000421027.1:p.Ala420Ser
ENST00000505649.5:n.1255G>T
ENST00000508932.5:n.175+107G>T
ENST00000509063.5:c.1708G>T	ENSP00000422784.1:p.Ala570Ser
ENST00000511370.1:c.1241G>T
ENST00000621085.4:c.1069G>T	ENSP00000483421.1:p.Ala357Ser
ENST00000621628.4:c.1069G>T	ENSP00000480485.1:p.Ala357Ser
NM_000477.5:c.1708G>T	NP_000468.1:p.Ala570Ser
NM_000477.6:c.1708G>T	NP_000468.1:p.Ala570Ser
NM_000477.7:c.1708G>T MANE Select	NP_000468.1:p.Ala570Ser