Canonical Allele Identifier: CA475482690
Gene: CATSPER1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.65792726G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025255G>C , CM000673.2:g.66025255G>C GRCh38
NC_000011.9:g.65792726G>C , CM000673.1:g.65792726G>C GRCh37
NC_000011.8:g.65549302G>C NCBI36
NG_016285.1:g.6263C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312106.6:c.1125C>G MANE Select ENSP00000309052.5:p.Thr375=
ENST00000312106.5:c.1125C>G ENSP00000309052.5:p.Thr375=
NM_053054.3:c.1125C>G NP_444282.3:p.Thr375=
XR_949785.1:n.1265C>G
XR_949786.1:n.1265C>G
XR_949787.1:n.1265C>G
XR_002957121.1:n.1263C>G
XR_002957122.1:n.1264C>G
XR_949785.2:n.1263C>G
XR_949787.2:n.1264C>G
NM_053054.4:c.1125C>G MANE Select NP_444282.3:p.Thr375=