Canonical Allele Identifier: CA357235531

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74272384C>T (hg19) ; chr4:g.73406667C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406667C>T , CM000666.2:g.73406667C>T	GRCh38
NC_000004.11:g.74272384C>T , CM000666.1:g.74272384C>T	GRCh37
NC_000004.10:g.74491248C>T	NCBI36
NG_009291.1:g.7413C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.176C>T MANE Select	ENSP00000295897.4:p.Pro59Leu
ENST00000295897.8:c.176C>T	ENSP00000295897.4:p.Pro59Leu
ENST00000401494.7:c.137+1494C>T	ENSP00000384695.3:n.137+1494C>T
ENST00000415165.6:c.137+1494C>T	ENSP00000401820.2:n.137+1494C>T
ENST00000441319.5:c.182C>T	ENSP00000392541.1:p.Pro61Leu
ENST00000476441.6:c.79+2261C>T	ENSP00000423727.1:n.79+2261C>T
ENST00000503124.5:c.-63C>T	ENSP00000421027.1:n.-63C>T
ENST00000509063.5:c.176C>T	ENSP00000422784.1:p.Pro59Leu
ENST00000510166.5:n.212C>T
ENST00000514786.1:n.145C>T
ENST00000515133.5:n.217C>T
ENST00000621085.4:c.176C>T	ENSP00000483421.1:p.Pro59Leu
ENST00000621628.4:c.176C>T	ENSP00000480485.1:p.Pro59Leu
NM_000477.5:c.176C>T	NP_000468.1:p.Pro59Leu
NM_000477.6:c.176C>T	NP_000468.1:p.Pro59Leu
NM_000477.7:c.176C>T MANE Select	NP_000468.1:p.Pro59Leu