Canonical Allele Identifier: CA357241182

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280798C>A (hg19) ; chr4:g.73415081C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415081C>A , CM000666.2:g.73415081C>A	GRCh38
NC_000004.11:g.74280798C>A , CM000666.1:g.74280798C>A	GRCh37
NC_000004.10:g.74499662C>A	NCBI36
NG_009291.1:g.15827C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1105C>A MANE Select	ENSP00000295897.4:p.Leu369Met
ENST00000295897.8:c.1105C>A	ENSP00000295897.4:p.Leu369Met
ENST00000401494.7:c.760C>A	ENSP00000384695.3:p.Leu254Met
ENST00000415165.6:c.529C>A	ENSP00000401820.2:p.Leu177Met
ENST00000476441.6:c.*384C>A	ENSP00000423727.1:n.*384C>A
ENST00000484992.1:n.425C>A
ENST00000503124.5:c.655C>A	ENSP00000421027.1:p.Leu219Met
ENST00000504043.1:n.108C>A
ENST00000505649.5:n.791C>A
ENST00000509063.5:c.1105C>A	ENSP00000422784.1:p.Leu369Met
ENST00000511370.1:c.638C>A
ENST00000621085.4:c.491-25C>A	ENSP00000483421.1:n.491-25C>A
ENST00000621628.4:c.487-21C>A	ENSP00000480485.1:n.487-21C>A
NM_000477.5:c.1105C>A	NP_000468.1:p.Leu369Met
NM_000477.6:c.1105C>A	NP_000468.1:p.Leu369Met
NM_000477.7:c.1105C>A MANE Select	NP_000468.1:p.Leu369Met