Canonical Allele Identifier: CA357241426

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280849G>C (hg19) ; chr4:g.73415132G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415132G>C , CM000666.2:g.73415132G>C	GRCh38
NC_000004.11:g.74280849G>C , CM000666.1:g.74280849G>C	GRCh37
NC_000004.10:g.74499713G>C	NCBI36
NG_009291.1:g.15878G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1156G>C MANE Select	ENSP00000295897.4:p.Ala386Pro
ENST00000295897.8:c.1156G>C	ENSP00000295897.4:p.Ala386Pro
ENST00000401494.7:c.811G>C	ENSP00000384695.3:p.Ala271Pro
ENST00000415165.6:c.580G>C	ENSP00000401820.2:p.Ala194Pro
ENST00000476441.6:c.*435G>C	ENSP00000423727.1:n.*435G>C
ENST00000484992.1:n.476G>C
ENST00000503124.5:c.706G>C	ENSP00000421027.1:p.Ala236Pro
ENST00000504043.1:n.159G>C
ENST00000505649.5:n.842G>C
ENST00000509063.5:c.1156G>C	ENSP00000422784.1:p.Ala386Pro
ENST00000511370.1:c.689G>C
ENST00000621085.4:c.517G>C	ENSP00000483421.1:p.Ala173Pro
ENST00000621628.4:c.517G>C	ENSP00000480485.1:p.Ala173Pro
NM_000477.5:c.1156G>C	NP_000468.1:p.Ala386Pro
NM_000477.6:c.1156G>C	NP_000468.1:p.Ala386Pro
NM_000477.7:c.1156G>C MANE Select	NP_000468.1:p.Ala386Pro