Canonical Allele Identifier: CA357246169

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285258G>C (hg19) ; chr4:g.73419541G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419541G>C , CM000666.2:g.73419541G>C	GRCh38
NC_000004.11:g.74285258G>C , CM000666.1:g.74285258G>C	GRCh37
NC_000004.10:g.74504122G>C	NCBI36
NG_009291.1:g.20287G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1687G>C MANE Select	ENSP00000295897.4:p.Ala563Pro
ENST00000295897.8:c.1687G>C	ENSP00000295897.4:p.Ala563Pro
ENST00000401494.7:c.1342G>C	ENSP00000384695.3:p.Ala448Pro
ENST00000415165.6:c.1111G>C	ENSP00000401820.2:p.Ala371Pro
ENST00000476441.6:c.*966G>C	ENSP00000423727.1:n.*966G>C
ENST00000486939.1:n.341G>C
ENST00000503124.5:c.1237G>C	ENSP00000421027.1:p.Ala413Pro
ENST00000505649.5:n.1234G>C
ENST00000508932.5:n.175+86G>C
ENST00000509063.5:c.1687G>C	ENSP00000422784.1:p.Ala563Pro
ENST00000511370.1:c.1220G>C
ENST00000621085.4:c.1048G>C	ENSP00000483421.1:p.Ala350Pro
ENST00000621628.4:c.1048G>C	ENSP00000480485.1:p.Ala350Pro
NM_000477.5:c.1687G>C	NP_000468.1:p.Ala563Pro
NM_000477.6:c.1687G>C	NP_000468.1:p.Ala563Pro
NM_000477.7:c.1687G>C MANE Select	NP_000468.1:p.Ala563Pro