Canonical Allele Identifier: CA357241276

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280822T>G (hg19) ; chr4:g.73415105T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415105T>G , CM000666.2:g.73415105T>G	GRCh38
NC_000004.11:g.74280822T>G , CM000666.1:g.74280822T>G	GRCh37
NC_000004.10:g.74499686T>G	NCBI36
NG_009291.1:g.15851T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1129T>G MANE Select	ENSP00000295897.4:p.Tyr377Asp
ENST00000295897.8:c.1129T>G	ENSP00000295897.4:p.Tyr377Asp
ENST00000401494.7:c.784T>G	ENSP00000384695.3:p.Tyr262Asp
ENST00000415165.6:c.553T>G	ENSP00000401820.2:p.Tyr185Asp
ENST00000476441.6:c.*408T>G	ENSP00000423727.1:n.*408T>G
ENST00000484992.1:n.449T>G
ENST00000503124.5:c.679T>G	ENSP00000421027.1:p.Tyr227Asp
ENST00000504043.1:n.132T>G
ENST00000505649.5:n.815T>G
ENST00000509063.5:c.1129T>G	ENSP00000422784.1:p.Tyr377Asp
ENST00000511370.1:c.662T>G
ENST00000621085.4:c.491-1T>G	ENSP00000483421.1:n.491-1T>G
ENST00000621628.4:c.490T>G	ENSP00000480485.1:p.Tyr164Asp
NM_000477.5:c.1129T>G	NP_000468.1:p.Tyr377Asp
NM_000477.6:c.1129T>G	NP_000468.1:p.Tyr377Asp
NM_000477.7:c.1129T>G MANE Select	NP_000468.1:p.Tyr377Asp