Canonical Allele Identifier: CA357238092

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275104A>G (hg19) ; chr4:g.73409387A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409387A>G , CM000666.2:g.73409387A>G	GRCh38
NC_000004.11:g.74275104A>G , CM000666.1:g.74275104A>G	GRCh37
NC_000004.10:g.74493968A>G	NCBI36
NG_009291.1:g.10133A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.515A>G MANE Select	ENSP00000295897.4:p.Tyr172Cys
ENST00000295897.8:c.515A>G	ENSP00000295897.4:p.Tyr172Cys
ENST00000401494.7:c.170A>G	ENSP00000384695.3:p.Tyr57Cys
ENST00000415165.6:c.138-2609A>G	ENSP00000401820.2:n.138-2609A>G
ENST00000441319.5:c.521A>G	ENSP00000392541.1:p.Tyr174Cys
ENST00000476441.6:c.112A>G	ENSP00000423727.1:p.Thr38Ala
ENST00000503124.5:c.65A>G	ENSP00000421027.1:p.Tyr22Cys
ENST00000505649.5:n.201A>G
ENST00000509063.5:c.515A>G	ENSP00000422784.1:p.Tyr172Cys
ENST00000511370.1:c.48A>G
ENST00000514786.1:n.484A>G
ENST00000621085.4:c.490+25A>G	ENSP00000483421.1:n.490+25A>G
ENST00000621628.4:c.486+311A>G	ENSP00000480485.1:n.486+311A>G
NM_000477.5:c.515A>G	NP_000468.1:p.Tyr172Cys
NM_000477.6:c.515A>G	NP_000468.1:p.Tyr172Cys
NM_000477.7:c.515A>G MANE Select	NP_000468.1:p.Tyr172Cys