Canonical Allele Identifier: CA357244796

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283938A>G (hg19) ; chr4:g.73418221A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418221A>G , CM000666.2:g.73418221A>G	GRCh38
NC_000004.11:g.74283938A>G , CM000666.1:g.74283938A>G	GRCh37
NC_000004.10:g.74502802A>G	NCBI36
NG_009291.1:g.18967A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1562A>G MANE Select	ENSP00000295897.4:p.Tyr521Cys
ENST00000295897.8:c.1562A>G	ENSP00000295897.4:p.Tyr521Cys
ENST00000401494.7:c.1217A>G	ENSP00000384695.3:p.Tyr406Cys
ENST00000415165.6:c.986A>G	ENSP00000401820.2:p.Tyr329Cys
ENST00000476441.6:c.*841A>G	ENSP00000423727.1:n.*841A>G
ENST00000486939.1:n.216A>G
ENST00000503124.5:c.1112A>G	ENSP00000421027.1:p.Tyr371Cys
ENST00000505649.5:n.1109A>G
ENST00000509063.5:c.1562A>G	ENSP00000422784.1:p.Tyr521Cys
ENST00000511370.1:c.1095A>G
ENST00000621085.4:c.923A>G	ENSP00000483421.1:p.Tyr308Cys
ENST00000621628.4:c.923A>G	ENSP00000480485.1:p.Tyr308Cys
NM_000477.5:c.1562A>G	NP_000468.1:p.Tyr521Cys
NM_000477.6:c.1562A>G	NP_000468.1:p.Tyr521Cys
NM_000477.7:c.1562A>G MANE Select	NP_000468.1:p.Tyr521Cys