Canonical Allele Identifier: CA269671310

Gene: CHP1

Linked Data

• dbSNP Id: rs180923656
• MyVariant Identifiers: chr15:g.41271763C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41271763C>T , CM000677.2:g.41271763C>T	GRCh38
NC_000015.9:g.41563961C>T , CM000677.1:g.41563961C>T	GRCh37
NC_000015.8:g.39351253C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334660.10:c.411+1145C>T MANE Select	ENSP00000335632.5:n.411+1145C>T
ENST00000334660.9:c.411+1145C>T	ENSP00000335632.5:n.411+1145C>T
ENST00000392151.6:c.350-7004C>T	ENSP00000440490.1:n.350-7004C>T
ENST00000558351.5:n.543+1145C>T
ENST00000560397.5:c.411+1145C>T	ENSP00000454007.1:n.411+1145C>T
ENST00000560411.5:c.*176+1145C>T	ENSP00000453375.1:n.*176+1145C>T
ENST00000560633.1:n.399-417C>T
ENST00000560784.5:c.*110+1145C>T	ENSP00000452772.1:n.*110+1145C>T
ENST00000560965.1:c.272-417C>T
NM_007236.4:c.411+1145C>T	NP_009167.1:n.411+1145C>T
NM_007236.5:c.411+1145C>T MANE Select	NP_009167.1:n.411+1145C>T