Canonical Allele Identifier: CA357244271

Gene: ALB

Linked Data

• gnomAD v4: 4-73418134-C-A
• MyVariant Identifiers: chr4:g.74283851C>A (hg19) ; chr4:g.73418134C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418134C>A , CM000666.2:g.73418134C>A	GRCh38
NC_000004.11:g.74283851C>A , CM000666.1:g.74283851C>A	GRCh37
NC_000004.10:g.74502715C>A	NCBI36
NG_009291.1:g.18880C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1475C>A MANE Select	ENSP00000295897.4:p.Pro492Gln
ENST00000295897.8:c.1475C>A	ENSP00000295897.4:p.Pro492Gln
ENST00000401494.7:c.1130C>A	ENSP00000384695.3:p.Pro377Gln
ENST00000415165.6:c.899C>A	ENSP00000401820.2:p.Pro300Gln
ENST00000476441.6:c.*754C>A	ENSP00000423727.1:n.*754C>A
ENST00000486939.1:n.129C>A
ENST00000503124.5:c.1025C>A	ENSP00000421027.1:p.Pro342Gln
ENST00000505649.5:n.1022C>A
ENST00000509063.5:c.1475C>A	ENSP00000422784.1:p.Pro492Gln
ENST00000511370.1:c.1008C>A
ENST00000621085.4:c.836C>A	ENSP00000483421.1:p.Pro279Gln
ENST00000621628.4:c.836C>A	ENSP00000480485.1:p.Pro279Gln
NM_000477.5:c.1475C>A	NP_000468.1:p.Pro492Gln
NM_000477.6:c.1475C>A	NP_000468.1:p.Pro492Gln
NM_000477.7:c.1475C>A MANE Select	NP_000468.1:p.Pro492Gln