Canonical Allele Identifier: CA357244207
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73418119T>G , CM000666.2:g.73418119T>G GRCh38
NC_000004.11:g.74283836T>G , CM000666.1:g.74283836T>G GRCh37
NC_000004.10:g.74502700T>G NCBI36
NG_009291.1:g.18865T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1460T>G MANE Select ENSP00000295897.4:p.Leu487Trp
ENST00000295897.8:c.1460T>G ENSP00000295897.4:p.Leu487Trp
ENST00000401494.7:c.1115T>G ENSP00000384695.3:p.Leu372Trp
ENST00000415165.6:c.884T>G ENSP00000401820.2:p.Leu295Trp
ENST00000476441.6:c.*739T>G ENSP00000423727.1:n.*739T>G
ENST00000486939.1:n.114T>G
ENST00000503124.5:c.1010T>G ENSP00000421027.1:p.Leu337Trp
ENST00000505649.5:n.1007T>G
ENST00000509063.5:c.1460T>G ENSP00000422784.1:p.Leu487Trp
ENST00000511370.1:c.993T>G
ENST00000621085.4:c.821T>G ENSP00000483421.1:p.Leu274Trp
ENST00000621628.4:c.821T>G ENSP00000480485.1:p.Leu274Trp
NM_000477.5:c.1460T>G NP_000468.1:p.Leu487Trp
NM_000477.6:c.1460T>G NP_000468.1:p.Leu487Trp
NM_000477.7:c.1460T>G MANE Select NP_000468.1:p.Leu487Trp