Canonical Allele Identifier: CA357240557

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279180C>A (hg19) ; chr4:g.73413463C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413463C>A , CM000666.2:g.73413463C>A	GRCh38
NC_000004.11:g.74279180C>A , CM000666.1:g.74279180C>A	GRCh37
NC_000004.10:g.74498044C>A	NCBI36
NG_009291.1:g.14209C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.887C>A MANE Select	ENSP00000295897.4:p.Ser296Tyr
ENST00000295897.8:c.887C>A	ENSP00000295897.4:p.Ser296Tyr
ENST00000401494.7:c.542C>A	ENSP00000384695.3:p.Ser181Tyr
ENST00000415165.6:c.311C>A	ENSP00000401820.2:p.Ser104Tyr
ENST00000476441.6:c.*166C>A	ENSP00000423727.1:n.*166C>A
ENST00000484992.1:n.207C>A
ENST00000503124.5:c.437C>A	ENSP00000421027.1:p.Ser146Tyr
ENST00000505649.5:n.573C>A
ENST00000509063.5:c.887C>A	ENSP00000422784.1:p.Ser296Tyr
ENST00000511370.1:c.420C>A
ENST00000621085.4:c.491-1643C>A	ENSP00000483421.1:n.491-1643C>A
ENST00000621628.4:c.487-1639C>A	ENSP00000480485.1:n.487-1639C>A
NM_000477.5:c.887C>A	NP_000468.1:p.Ser296Tyr
NM_000477.6:c.887C>A	NP_000468.1:p.Ser296Tyr
NM_000477.7:c.887C>A MANE Select	NP_000468.1:p.Ser296Tyr