Canonical Allele Identifier: CA357241633

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280882G>A (hg19) ; chr4:g.73415165G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415165G>A , CM000666.2:g.73415165G>A	GRCh38
NC_000004.11:g.74280882G>A , CM000666.1:g.74280882G>A	GRCh37
NC_000004.10:g.74499746G>A	NCBI36
NG_009291.1:g.15911G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1189G>A MANE Select	ENSP00000295897.4:p.Val397Met
ENST00000295897.8:c.1189G>A	ENSP00000295897.4:p.Val397Met
ENST00000401494.7:c.844G>A	ENSP00000384695.3:p.Val282Met
ENST00000415165.6:c.613G>A	ENSP00000401820.2:p.Val205Met
ENST00000476441.6:c.*468G>A	ENSP00000423727.1:n.*468G>A
ENST00000484992.1:n.509G>A
ENST00000503124.5:c.739G>A	ENSP00000421027.1:p.Val247Met
ENST00000504043.1:n.192G>A
ENST00000505649.5:n.875G>A
ENST00000509063.5:c.1189G>A	ENSP00000422784.1:p.Val397Met
ENST00000511370.1:c.722G>A
ENST00000621085.4:c.550G>A	ENSP00000483421.1:p.Val184Met
ENST00000621628.4:c.550G>A	ENSP00000480485.1:p.Val184Met
NM_000477.5:c.1189G>A	NP_000468.1:p.Val397Met
NM_000477.6:c.1189G>A	NP_000468.1:p.Val397Met
NM_000477.7:c.1189G>A MANE Select	NP_000468.1:p.Val397Met