Canonical Allele Identifier: CA439799527

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275180T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409463T>C , CM000666.2:g.73409463T>C	GRCh38
NC_000004.11:g.74275180T>C , CM000666.1:g.74275180T>C	GRCh37
NC_000004.10:g.74494044T>C	NCBI36
NG_009291.1:g.10209T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.591T>C MANE Select	ENSP00000295897.4:p.Asp197=
ENST00000295897.8:c.591T>C	ENSP00000295897.4:p.Asp197=
ENST00000401494.7:c.246T>C	ENSP00000384695.3:p.Asp82=
ENST00000415165.6:c.138-2533T>C	ENSP00000401820.2:n.138-2533T>C
ENST00000476441.6:c.188T>C	ENSP00000423727.1:p.Ile63Thr
ENST00000503124.5:c.141T>C	ENSP00000421027.1:p.Asp47=
ENST00000505649.5:n.277T>C
ENST00000509063.5:c.591T>C	ENSP00000422784.1:p.Asp197=
ENST00000511370.1:c.124T>C
ENST00000514786.1:n.560T>C
ENST00000621085.4:c.490+101T>C	ENSP00000483421.1:n.490+101T>C
ENST00000621628.4:c.486+387T>C	ENSP00000480485.1:n.486+387T>C
NM_000477.5:c.591T>C	NP_000468.1:p.Asp197=
NM_000477.6:c.591T>C	NP_000468.1:p.Asp197=
NM_000477.7:c.591T>C MANE Select	NP_000468.1:p.Asp197=