Canonical Allele Identifier: CA357247297

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74286008G>T (hg19) ; chr4:g.73420291G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420291G>T , CM000666.2:g.73420291G>T	GRCh38
NC_000004.11:g.74286008G>T , CM000666.1:g.74286008G>T	GRCh37
NC_000004.10:g.74504872G>T	NCBI36
NG_009291.1:g.21037G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1823G>T MANE Select	ENSP00000295897.4:p.Gly608Val
ENST00000295897.8:c.1823G>T	ENSP00000295897.4:p.Gly608Val
ENST00000401494.7:c.1478G>T	ENSP00000384695.3:p.Gly493Val
ENST00000415165.6:c.1247G>T	ENSP00000401820.2:p.Gly416Val
ENST00000476441.6:c.*1102G>T	ENSP00000423727.1:n.*1102G>T
ENST00000495173.1:n.131G>T
ENST00000503124.5:c.1373G>T	ENSP00000421027.1:p.Gly458Val
ENST00000505649.5:n.1370G>T
ENST00000508932.5:n.213G>T
ENST00000509063.5:c.1785+652G>T	ENSP00000422784.1:n.1785+652G>T
ENST00000511370.1:c.1356G>T
ENST00000621085.4:c.1184G>T	ENSP00000483421.1:p.Gly395Val
ENST00000621628.4:c.1184G>T	ENSP00000480485.1:p.Gly395Val
NM_000477.5:c.1823G>T	NP_000468.1:p.Gly608Val
NM_000477.6:c.1823G>T	NP_000468.1:p.Gly608Val
NM_000477.7:c.1823G>T MANE Select	NP_000468.1:p.Gly608Val