Canonical Allele Identifier: CA357241459

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280855G>C (hg19) ; chr4:g.73415138G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415138G>C , CM000666.2:g.73415138G>C	GRCh38
NC_000004.11:g.74280855G>C , CM000666.1:g.74280855G>C	GRCh37
NC_000004.10:g.74499719G>C	NCBI36
NG_009291.1:g.15884G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1162G>C MANE Select	ENSP00000295897.4:p.Ala388Pro
ENST00000295897.8:c.1162G>C	ENSP00000295897.4:p.Ala388Pro
ENST00000401494.7:c.817G>C	ENSP00000384695.3:p.Ala273Pro
ENST00000415165.6:c.586G>C	ENSP00000401820.2:p.Ala196Pro
ENST00000476441.6:c.*441G>C	ENSP00000423727.1:n.*441G>C
ENST00000484992.1:n.482G>C
ENST00000503124.5:c.712G>C	ENSP00000421027.1:p.Ala238Pro
ENST00000504043.1:n.165G>C
ENST00000505649.5:n.848G>C
ENST00000509063.5:c.1162G>C	ENSP00000422784.1:p.Ala388Pro
ENST00000511370.1:c.695G>C
ENST00000621085.4:c.523G>C	ENSP00000483421.1:p.Ala175Pro
ENST00000621628.4:c.523G>C	ENSP00000480485.1:p.Ala175Pro
NM_000477.5:c.1162G>C	NP_000468.1:p.Ala388Pro
NM_000477.6:c.1162G>C	NP_000468.1:p.Ala388Pro
NM_000477.7:c.1162G>C MANE Select	NP_000468.1:p.Ala388Pro