Canonical Allele Identifier: CA357244266

Gene: ALB

Linked Data

• gnomAD v4: 4-73418133-C-G
• MyVariant Identifiers: chr4:g.74283850C>G (hg19) ; chr4:g.73418133C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418133C>G , CM000666.2:g.73418133C>G	GRCh38
NC_000004.11:g.74283850C>G , CM000666.1:g.74283850C>G	GRCh37
NC_000004.10:g.74502714C>G	NCBI36
NG_009291.1:g.18879C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1474C>G MANE Select	ENSP00000295897.4:p.Pro492Ala
ENST00000295897.8:c.1474C>G	ENSP00000295897.4:p.Pro492Ala
ENST00000401494.7:c.1129C>G	ENSP00000384695.3:p.Pro377Ala
ENST00000415165.6:c.898C>G	ENSP00000401820.2:p.Pro300Ala
ENST00000476441.6:c.*753C>G	ENSP00000423727.1:n.*753C>G
ENST00000486939.1:n.128C>G
ENST00000503124.5:c.1024C>G	ENSP00000421027.1:p.Pro342Ala
ENST00000505649.5:n.1021C>G
ENST00000509063.5:c.1474C>G	ENSP00000422784.1:p.Pro492Ala
ENST00000511370.1:c.1007C>G
ENST00000621085.4:c.835C>G	ENSP00000483421.1:p.Pro279Ala
ENST00000621628.4:c.835C>G	ENSP00000480485.1:p.Pro279Ala
NM_000477.5:c.1474C>G	NP_000468.1:p.Pro492Ala
NM_000477.6:c.1474C>G	NP_000468.1:p.Pro492Ala
NM_000477.7:c.1474C>G MANE Select	NP_000468.1:p.Pro492Ala