Canonical Allele Identifier: CA2742038357

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.[73404394C>T;73413606G>A] , CM000666.2:g.[73404394C>T;73413606G>A]	GRCh38
NC_000004.11:g.[74270111C>T;74279323G>A] , CM000666.1:g.[74270111C>T;74279323G>A]	GRCh37
NC_000004.10:g.[74488975C>T;74498187G>A]	NCBI36
NG_009291.1:g.[5140C>T;14352G>A]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.[67C>T;1030G>A] MANE Select	ENSP00000295897.4:p.[Arg23Cys;Ala344Thr]
ENST00000295897.8:c.[67C>T;1030G>A]	ENSP00000295897.4:p.[Arg23Cys;Ala344Thr]
ENST00000401494.7:c.[67C>T;685G>A]	ENSP00000384695.3:p.[Arg23Cys;Ala229Thr]
ENST00000415165.6:c.[67C>T;454G>A]	ENSP00000401820.2:p.[Arg23Cys;Ala152Thr]
ENST00000476441.6:c.[67C>T;*309G>A]	ENSP00000423727.1:[p.Arg23Cys;n.*309G>A]
ENST00000503124.5:c.[-114C>T;580G>A]	ENSP00000421027.1:p.Ala194Thr
ENST00000509063.5:c.[67C>T;1030G>A]	ENSP00000422784.1:p.[Arg23Cys;Ala344Thr]
ENST00000621085.4:c.[67C>T;491-1500G>A]	ENSP00000483421.1:p.Arg23Cys
ENST00000621628.4:c.[67C>T;487-1496G>A]	ENSP00000480485.1:p.Arg23Cys
NM_000477.5:c.[67C>T;1030G>A]	NP_000468.1:p.[Arg23Cys;Ala344Thr]
NM_000477.6:c.[67C>T;1030G>A]	NP_000468.1:p.[Arg23Cys;Ala344Thr]
NM_000477.7:c.[67C>T;1030G>A] MANE Select	NP_000468.1:p.[Arg23Cys;Ala344Thr]