Canonical Allele Identifier: CA388849628

Gene: CHAMP1

Linked Data

• dbSNP Id: rs2087238726
• gnomAD v4: 13-114325602-T-C
• MyVariant Identifiers: chr13:g.115091077T>C (hg19) ; chr13:g.114325602T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.114325602T>C , CM000675.2:g.114325602T>C	GRCh38
NC_000013.10:g.115091077T>C , CM000675.1:g.115091077T>C	GRCh37
NC_000013.9:g.114109179T>C	NCBI36
NG_051829.1:g.16268T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643483.2:c.1760T>C	ENSP00000496699.1:p.Ile587Thr
ENST00000644294.2:c.1760T>C	ENSP00000495985.2:p.Ile587Thr
ENST00000645174.2:c.1760T>C	ENSP00000494031.2:p.Ile587Thr
ENST00000700527.1:c.1760T>C	ENSP00000515032.1:p.Ile587Thr
ENST00000700528.1:c.1760T>C	ENSP00000515033.1:p.Ile587Thr
ENST00000361283.4:c.1760T>C MANE Select	ENSP00000354730.1:p.Ile587Thr
ENST00000643483.1:c.1760T>C	ENSP00000496699.1:p.Ile587Thr
ENST00000646155.1:n.123+10959T>C
ENST00000646956.1:n.285+4370T>C
ENST00000361283.2:c.1760T>C	ENSP00000354730.1:p.Ile587Thr
NM_001164144.1:c.1760T>C	NP_001157616.1:p.Ile587Thr
NM_001164145.1:c.1760T>C	NP_001157617.1:p.Ile587Thr
NM_032436.2:c.1760T>C	NP_115812.1:p.Ile587Thr
NM_001164144.2:c.1760T>C	NP_001157616.1:p.Ile587Thr
NM_001164145.2:c.1760T>C	NP_001157617.1:p.Ile587Thr
NM_032436.3:c.1760T>C	NP_115812.1:p.Ile587Thr
NM_032436.4:c.1760T>C MANE Select	NP_115812.1:p.Ile587Thr
NM_001164144.3:c.1760T>C	NP_001157616.1:p.Ile587Thr
NM_001164145.3:c.1760T>C	NP_001157617.1:p.Ile587Thr