Canonical Allele Identifier: CA15649846

Gene: ZNF438

Linked Data

• dbSNP Id: rs1690625
• gnomAD v2: 10-31295821-C-G
• gnomAD v3: 10-31006892-C-G
• gnomAD v4: 10-31006892-C-G
• MyVariant Identifiers: chr10:g.31295821C>G (hg19) ; chr10:g.31006892C>G (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.31006892C>G , CM000672.2:g.31006892C>G	GRCh38
NC_000010.10:g.31295821C>G , CM000672.1:g.31295821C>G	GRCh37
NC_000010.9:g.31335827C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000436087.7:c.-249-22466G>C MANE Select	ENSP00000406934.2:n.-249-22466G>C
ENST00000375311.1:c.-722+24941G>C	ENSP00000364460.1:n.-722+24941G>C
ENST00000413025.5:c.-192+24941G>C	ENSP00000387546.1:n.-192+24941G>C
ENST00000436087.6:c.-249-22466G>C	ENSP00000406934.2:n.-249-22466G>C
ENST00000442986.5:c.-330-22466G>C	ENSP00000412363.1:n.-330-22466G>C
ENST00000452305.5:c.-459-22466G>C	ENSP00000413060.1:n.-459-22466G>C
NM_001143766.1:c.-378-22466G>C	NP_001137238.1:n.-378-22466G>C
NM_001143767.1:c.-192+24941G>C	NP_001137239.1:n.-192+24941G>C
NM_001143768.1:c.-249-22466G>C	NP_001137240.1:n.-249-22466G>C
NM_001143770.1:c.-459-22466G>C	NP_001137242.1:n.-459-22466G>C
NM_001143771.1:c.-430-22466G>C	NP_001137243.1:n.-430-22466G>C
NM_182755.2:c.-330-22466G>C	NP_877432.1:n.-330-22466G>C
NR_026560.1:n.105+24941G>C
XM_006717394.2:c.-231-22466G>C	XP_006717457.1:n.-231-22466G>C
XM_006717396.2:c.-115+24941G>C	XP_006717459.1:n.-115+24941G>C
XM_006717398.2:c.-437-22466G>C	XP_006717461.1:n.-437-22466G>C
XM_006717399.2:c.-378-22466G>C	XP_006717462.1:n.-378-22466G>C
XM_011519372.1:c.-249-22466G>C	XP_011517674.1:n.-249-22466G>C
XM_011519375.1:c.-507-22466G>C	XP_011517677.1:n.-507-22466G>C
XM_011519376.1:c.-557-22466G>C	XP_011517678.1:n.-557-22466G>C
XM_011519377.1:c.-553-22466G>C	XP_011517679.1:n.-553-22466G>C
XM_006717396.3:c.-115+24941G>C	XP_006717459.1:n.-115+24941G>C
XM_006717398.3:c.-437-22466G>C	XP_006717461.1:n.-437-22466G>C
XM_006717399.3:c.-378-22466G>C	XP_006717462.1:n.-378-22466G>C
XM_011519372.2:c.-249-22466G>C	XP_011517674.1:n.-249-22466G>C
XM_011519376.2:c.-557-22466G>C	XP_011517678.1:n.-557-22466G>C
XM_011519377.2:c.-553-22466G>C	XP_011517679.1:n.-553-22466G>C
XM_017015866.1:c.-426-22466G>C	XP_016871355.1:n.-426-22466G>C
XM_017015868.1:c.-172-22466G>C	XP_016871357.1:n.-172-22466G>C
XM_017015870.2:c.-302+16528G>C	XP_016871359.1:n.-302+16528G>C
XM_017015871.2:c.-166-22466G>C	XP_016871360.1:n.-166-22466G>C
XM_017015874.2:c.-244+24941G>C	XP_016871363.1:n.-244+24941G>C
XM_017015875.1:c.-779-22466G>C	XP_016871364.1:n.-779-22466G>C
XM_017015876.1:c.-989-22466G>C	XP_016871365.1:n.-989-22466G>C
XM_017015877.1:c.-958-22466G>C	XP_016871366.1:n.-958-22466G>C
XM_017015878.1:c.-821+24941G>C	XP_016871367.1:n.-821+24941G>C
XM_017015879.1:c.-901+24941G>C	XP_016871368.1:n.-901+24941G>C
XM_017015880.2:c.-702-22466G>C	XP_016871369.1:n.-702-22466G>C
XM_017015881.1:c.-645+24941G>C	XP_016871370.1:n.-645+24941G>C
XM_017015882.1:c.-744+24941G>C	XP_016871371.1:n.-744+24941G>C
XM_024447868.1:c.-459-22466G>C	XP_024303636.1:n.-459-22466G>C
XM_024447870.1:c.-308-22466G>C	XP_024303638.1:n.-308-22466G>C
XM_024447871.1:c.-192+25279G>C	XP_024303639.1:n.-192+25279G>C
XM_024447872.1:c.-273+24941G>C	XP_024303640.1:n.-273+24941G>C
XM_024447873.1:c.-341+24941G>C	XP_024303641.1:n.-341+24941G>C
XM_024447875.1:c.-708-22466G>C	XP_024303643.1:n.-708-22466G>C
NM_001143766.2:c.-378-22466G>C	NP_001137238.1:n.-378-22466G>C
NM_001143767.2:c.-192+24941G>C	NP_001137239.1:n.-192+24941G>C
NM_001143768.2:c.-249-22466G>C MANE Select	NP_001137240.1:n.-249-22466G>C
NM_001143770.2:c.-459-22466G>C	NP_001137242.1:n.-459-22466G>C
NM_001143771.2:c.-430-22466G>C	NP_001137243.1:n.-430-22466G>C
NM_001387411.1:c.-115+24941G>C	NP_001374340.1:n.-115+24941G>C
NM_001387412.1:c.-172-22466G>C	NP_001374341.1:n.-172-22466G>C
NM_182755.3:c.-330-22466G>C	NP_877432.1:n.-330-22466G>C
NR_026560.2:n.33+24941G>C
NR_170659.1:n.33+24941G>C
NR_170660.1:n.33+24941G>C