Canonical Allele Identifier: CA357238326

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275181A>C (hg19) ; chr4:g.73409464A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409464A>C , CM000666.2:g.73409464A>C	GRCh38
NC_000004.11:g.74275181A>C , CM000666.1:g.74275181A>C	GRCh37
NC_000004.10:g.74494045A>C	NCBI36
NG_009291.1:g.10210A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.592A>C MANE Select	ENSP00000295897.4:p.Lys198Gln
ENST00000295897.8:c.592A>C	ENSP00000295897.4:p.Lys198Gln
ENST00000401494.7:c.247A>C	ENSP00000384695.3:p.Lys83Gln
ENST00000415165.6:c.138-2532A>C	ENSP00000401820.2:n.138-2532A>C
ENST00000476441.6:c.189A>C	ENSP00000423727.1:p.Ile63=
ENST00000503124.5:c.142A>C	ENSP00000421027.1:p.Lys48Gln
ENST00000505649.5:n.278A>C
ENST00000509063.5:c.592A>C	ENSP00000422784.1:p.Lys198Gln
ENST00000511370.1:c.125A>C
ENST00000514786.1:n.561A>C
ENST00000621085.4:c.490+102A>C	ENSP00000483421.1:n.490+102A>C
ENST00000621628.4:c.486+388A>C	ENSP00000480485.1:n.486+388A>C
NM_000477.5:c.592A>C	NP_000468.1:p.Lys198Gln
NM_000477.6:c.592A>C	NP_000468.1:p.Lys198Gln
NM_000477.7:c.592A>C MANE Select	NP_000468.1:p.Lys198Gln