Canonical Allele Identifier: CA357241084
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415050T>G , CM000666.2:g.73415050T>G GRCh38
NC_000004.11:g.74280767T>G , CM000666.1:g.74280767T>G GRCh37
NC_000004.10:g.74499631T>G NCBI36
NG_009291.1:g.15796T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1074T>G MANE Select ENSP00000295897.4:p.Tyr358Ter
ENST00000295897.8:c.1074T>G ENSP00000295897.4:p.Tyr358Ter
ENST00000401494.7:c.729T>G ENSP00000384695.3:p.Tyr243Ter
ENST00000415165.6:c.498T>G ENSP00000401820.2:p.Tyr166Ter
ENST00000476441.6:c.*353T>G ENSP00000423727.1:n.*353T>G
ENST00000484992.1:n.394T>G
ENST00000503124.5:c.624T>G ENSP00000421027.1:p.Tyr208Ter
ENST00000504043.1:n.77T>G
ENST00000505649.5:n.760T>G
ENST00000509063.5:c.1074T>G ENSP00000422784.1:p.Tyr358Ter
ENST00000511370.1:c.607T>G
ENST00000621085.4:c.491-56T>G ENSP00000483421.1:n.491-56T>G
ENST00000621628.4:c.487-52T>G ENSP00000480485.1:n.487-52T>G
NM_000477.5:c.1074T>G NP_000468.1:p.Tyr358Ter
NM_000477.6:c.1074T>G NP_000468.1:p.Tyr358Ter
NM_000477.7:c.1074T>G MANE Select NP_000468.1:p.Tyr358Ter