Canonical Allele Identifier: CA439799148

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274461A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408744A>C , CM000666.2:g.73408744A>C	GRCh38
NC_000004.11:g.74274461A>C , CM000666.1:g.74274461A>C	GRCh37
NC_000004.10:g.74493325A>C	NCBI36
NG_009291.1:g.9490A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.421A>C MANE Select	ENSP00000295897.4:p.Arg141=
ENST00000295897.8:c.421A>C	ENSP00000295897.4:p.Arg141=
ENST00000401494.7:c.138-611A>C	ENSP00000384695.3:n.138-611A>C
ENST00000415165.6:c.138-3252A>C	ENSP00000401820.2:n.138-3252A>C
ENST00000441319.5:c.427A>C	ENSP00000392541.1:p.Arg143=
ENST00000476441.6:c.80-611A>C	ENSP00000423727.1:n.80-611A>C
ENST00000503124.5:c.33-611A>C	ENSP00000421027.1:n.33-611A>C
ENST00000505649.5:n.107A>C
ENST00000509063.5:c.421A>C	ENSP00000422784.1:p.Arg141=
ENST00000510166.5:n.457A>C
ENST00000514786.1:n.390A>C
ENST00000515133.5:n.462A>C
ENST00000621085.4:c.421A>C	ENSP00000483421.1:p.Arg141=
ENST00000621628.4:c.421A>C	ENSP00000480485.1:p.Arg141=
NM_000477.5:c.421A>C	NP_000468.1:p.Arg141=
NM_000477.6:c.421A>C	NP_000468.1:p.Arg141=
NM_000477.7:c.421A>C MANE Select	NP_000468.1:p.Arg141=