Canonical Allele Identifier: CA11516521
Gene: NCEH1 HGNC NCBI

Linked Data

dbSNP Id: rs11712263

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172667903C>T , CM000665.2:g.172667903C>T GRCh38
NC_000003.11:g.172385693C>T , CM000665.1:g.172385693C>T GRCh37
NC_000003.10:g.173868387C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000421723.2:c.139-22211G>A ENSP00000402196.2:n.139-22211G>A
ENST00000424772.2:c.139-19789G>A ENSP00000392934.2:n.139-19789G>A
ENST00000475381.7:c.139-19789G>A MANE Select ENSP00000418571.4:n.139-19789G>A
ENST00000421723.1:c.235-22211G>A ENSP00000402196.1:n.235-22211G>A
ENST00000424772.1:c.207-19789G>A
ENST00000475381.5:c.235-19789G>A ENSP00000418571.2:n.235-19789G>A
ENST00000538775.5:c.235-19789G>A ENSP00000442464.1:n.235-19789G>A
ENST00000543711.5:c.-32-22211G>A ENSP00000443227.1:n.-32-22211G>A
NM_001146276.1:c.235-19789G>A NP_001139748.1:n.235-19789G>A
NM_001146277.1:c.-251-19789G>A NP_001139749.1:n.-251-19789G>A
NM_001146278.1:c.-32-22211G>A NP_001139750.1:n.-32-22211G>A
NM_020792.4:c.235-19789G>A NP_065843.3:n.235-19789G>A
NM_001146276.2:c.139-19789G>A NP_001139748.2:n.139-19789G>A
NM_001146277.2:c.-251-19789G>A NP_001139749.1:n.-251-19789G>A
NM_001146278.2:c.-32-22211G>A NP_001139750.1:n.-32-22211G>A
NM_020792.5:c.139-19789G>A NP_065843.4:n.139-19789G>A
NM_001146276.3:c.139-19789G>A NP_001139748.2:n.139-19789G>A
NM_001146277.3:c.-251-19789G>A NP_001139749.1:n.-251-19789G>A
NM_020792.6:c.139-19789G>A MANE Select NP_065843.4:n.139-19789G>A
NM_001146278.3:c.-32-22211G>A NP_001139750.1:n.-32-22211G>A