Canonical Allele Identifier: CA388847463

Gene: CHAMP1

Linked Data

• gnomAD v4: 13-114324794-G-C
• MyVariant Identifiers: chr13:g.115090269G>C (hg19) ; chr13:g.114324794G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.114324794G>C , CM000675.2:g.114324794G>C	GRCh38
NC_000013.10:g.115090269G>C , CM000675.1:g.115090269G>C	GRCh37
NC_000013.9:g.114108371G>C	NCBI36
NG_051829.1:g.15460G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000643483.2:c.952G>C	ENSP00000496699.1:p.Gly318Arg
ENST00000644294.2:c.952G>C	ENSP00000495985.2:p.Gly318Arg
ENST00000645174.2:c.952G>C	ENSP00000494031.2:p.Gly318Arg
ENST00000700527.1:c.952G>C	ENSP00000515032.1:p.Gly318Arg
ENST00000700528.1:c.952G>C	ENSP00000515033.1:p.Gly318Arg
ENST00000361283.4:c.952G>C MANE Select	ENSP00000354730.1:p.Gly318Arg
ENST00000643483.1:c.952G>C	ENSP00000496699.1:p.Gly318Arg
ENST00000646155.1:n.123+10151G>C
ENST00000646956.1:n.285+3562G>C
ENST00000361283.2:c.952G>C	ENSP00000354730.1:p.Gly318Arg
NM_001164144.1:c.952G>C	NP_001157616.1:p.Gly318Arg
NM_001164145.1:c.952G>C	NP_001157617.1:p.Gly318Arg
NM_032436.2:c.952G>C	NP_115812.1:p.Gly318Arg
NM_001164144.2:c.952G>C	NP_001157616.1:p.Gly318Arg
NM_001164145.2:c.952G>C	NP_001157617.1:p.Gly318Arg
NM_032436.3:c.952G>C	NP_115812.1:p.Gly318Arg
NM_032436.4:c.952G>C MANE Select	NP_115812.1:p.Gly318Arg
NM_001164144.3:c.952G>C	NP_001157616.1:p.Gly318Arg
NM_001164145.3:c.952G>C	NP_001157617.1:p.Gly318Arg