Canonical Allele Identifier: CA357241626

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280881A>C (hg19) ; chr4:g.73415164A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415164A>C , CM000666.2:g.73415164A>C	GRCh38
NC_000004.11:g.74280881A>C , CM000666.1:g.74280881A>C	GRCh37
NC_000004.10:g.74499745A>C	NCBI36
NG_009291.1:g.15910A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1188A>C MANE Select	ENSP00000295897.4:p.Lys396Asn
ENST00000295897.8:c.1188A>C	ENSP00000295897.4:p.Lys396Asn
ENST00000401494.7:c.843A>C	ENSP00000384695.3:p.Lys281Asn
ENST00000415165.6:c.612A>C	ENSP00000401820.2:p.Lys204Asn
ENST00000476441.6:c.*467A>C	ENSP00000423727.1:n.*467A>C
ENST00000484992.1:n.508A>C
ENST00000503124.5:c.738A>C	ENSP00000421027.1:p.Lys246Asn
ENST00000504043.1:n.191A>C
ENST00000505649.5:n.874A>C
ENST00000509063.5:c.1188A>C	ENSP00000422784.1:p.Lys396Asn
ENST00000511370.1:c.721A>C
ENST00000621085.4:c.549A>C	ENSP00000483421.1:p.Lys183Asn
ENST00000621628.4:c.549A>C	ENSP00000480485.1:p.Lys183Asn
NM_000477.5:c.1188A>C	NP_000468.1:p.Lys396Asn
NM_000477.6:c.1188A>C	NP_000468.1:p.Lys396Asn
NM_000477.7:c.1188A>C MANE Select	NP_000468.1:p.Lys396Asn