Canonical Allele Identifier: CA357247163

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285990C>T (hg19) ; chr4:g.73420273C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420273C>T , CM000666.2:g.73420273C>T	GRCh38
NC_000004.11:g.74285990C>T , CM000666.1:g.74285990C>T	GRCh37
NC_000004.10:g.74504854C>T	NCBI36
NG_009291.1:g.21019C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1805C>T MANE Select	ENSP00000295897.4:p.Ala602Val
ENST00000295897.8:c.1805C>T	ENSP00000295897.4:p.Ala602Val
ENST00000401494.7:c.1460C>T	ENSP00000384695.3:p.Ala487Val
ENST00000415165.6:c.1229C>T	ENSP00000401820.2:p.Ala410Val
ENST00000476441.6:c.*1084C>T	ENSP00000423727.1:n.*1084C>T
ENST00000495173.1:n.113C>T
ENST00000503124.5:c.1355C>T	ENSP00000421027.1:p.Ala452Val
ENST00000505649.5:n.1352C>T
ENST00000508932.5:n.195C>T
ENST00000509063.5:c.1785+634C>T	ENSP00000422784.1:n.1785+634C>T
ENST00000511370.1:c.1338C>T
ENST00000621085.4:c.1166C>T	ENSP00000483421.1:p.Ala389Val
ENST00000621628.4:c.1166C>T	ENSP00000480485.1:p.Ala389Val
NM_000477.5:c.1805C>T	NP_000468.1:p.Ala602Val
NM_000477.6:c.1805C>T	NP_000468.1:p.Ala602Val
NM_000477.7:c.1805C>T MANE Select	NP_000468.1:p.Ala602Val