Canonical Allele Identifier: CA2244625625

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933589T= , CM000679.2:g.4933589T= GRCh38
NC_000017.10:g.4836884T= , CM000679.1:g.4836884T= GRCh37
NC_000017.9:g.4777664T= NCBI36
NG_008767.2:g.6295T=

Transcript Alleles

HGVS Amino-acid change
ENST00000329125.6:c.985T= (GP1BA) MANE Select ENSP00000329380.5:p.Trp329=
ENST00000649830.1:c.-888+753A= (CHRNE) ENSP00000496907.1:n.-888+753A=
ENST00000329125.5:c.985T= (GP1BA) ENSP00000329380.5:p.Trp329=
ENST00000611961.1:c.985T= (GP1BA) ENSP00000484439.1:p.Trp329=
NM_000173.6:c.985T= (GP1BA) NP_000164.5:p.Trp329=
NM_000173.7:c.985T= (GP1BA) MANE Select NP_000164.5:p.Trp329=