Canonical Allele Identifier: CA357237212
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73408748C>T , CM000666.2:g.73408748C>T GRCh38
NC_000004.11:g.74274465C>T , CM000666.1:g.74274465C>T GRCh37
NC_000004.10:g.74493329C>T NCBI36
NG_009291.1:g.9494C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.425C>T MANE Select ENSP00000295897.4:p.Pro142Leu
ENST00000295897.8:c.425C>T ENSP00000295897.4:p.Pro142Leu
ENST00000401494.7:c.138-607C>T ENSP00000384695.3:n.138-607C>T
ENST00000415165.6:c.138-3248C>T ENSP00000401820.2:n.138-3248C>T
ENST00000441319.5:c.431C>T ENSP00000392541.1:p.Pro144Leu
ENST00000476441.6:c.80-607C>T ENSP00000423727.1:n.80-607C>T
ENST00000503124.5:c.33-607C>T ENSP00000421027.1:n.33-607C>T
ENST00000505649.5:n.111C>T
ENST00000509063.5:c.425C>T ENSP00000422784.1:p.Pro142Leu
ENST00000510166.5:n.461C>T
ENST00000514786.1:n.394C>T
ENST00000515133.5:n.466C>T
ENST00000621085.4:c.425C>T ENSP00000483421.1:p.Pro142Leu
ENST00000621628.4:c.425C>T ENSP00000480485.1:p.Pro142Leu
NM_000477.5:c.425C>T NP_000468.1:p.Pro142Leu
NM_000477.6:c.425C>T NP_000468.1:p.Pro142Leu
NM_000477.7:c.425C>T MANE Select NP_000468.1:p.Pro142Leu