Canonical Allele Identifier: CA357246148

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285255A>C (hg19) ; chr4:g.73419538A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419538A>C , CM000666.2:g.73419538A>C	GRCh38
NC_000004.11:g.74285255A>C , CM000666.1:g.74285255A>C	GRCh37
NC_000004.10:g.74504119A>C	NCBI36
NG_009291.1:g.20284A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1684A>C MANE Select	ENSP00000295897.4:p.Lys562Gln
ENST00000295897.8:c.1684A>C	ENSP00000295897.4:p.Lys562Gln
ENST00000401494.7:c.1339A>C	ENSP00000384695.3:p.Lys447Gln
ENST00000415165.6:c.1108A>C	ENSP00000401820.2:p.Lys370Gln
ENST00000476441.6:c.*963A>C	ENSP00000423727.1:n.*963A>C
ENST00000486939.1:n.338A>C
ENST00000503124.5:c.1234A>C	ENSP00000421027.1:p.Lys412Gln
ENST00000505649.5:n.1231A>C
ENST00000508932.5:n.175+83A>C
ENST00000509063.5:c.1684A>C	ENSP00000422784.1:p.Lys562Gln
ENST00000511370.1:c.1217A>C
ENST00000621085.4:c.1045A>C	ENSP00000483421.1:p.Lys349Gln
ENST00000621628.4:c.1045A>C	ENSP00000480485.1:p.Lys349Gln
NM_000477.5:c.1684A>C	NP_000468.1:p.Lys562Gln
NM_000477.6:c.1684A>C	NP_000468.1:p.Lys562Gln
NM_000477.7:c.1684A>C MANE Select	NP_000468.1:p.Lys562Gln