Canonical Allele Identifier: CA357241633
Gene: ALB HGNC NCBI

Linked Data

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