Canonical Allele Identifier: CA381336357
Gene: CATSPER1 HGNC NCBI

Linked Data

dbSNP Id: rs2134999406

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025252C>G , CM000673.2:g.66025252C>G GRCh38
NC_000011.9:g.65792723C>G , CM000673.1:g.65792723C>G GRCh37
NC_000011.8:g.65549299C>G NCBI36
NG_016285.1:g.6266G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000312106.6:c.1128G>C MANE Select ENSP00000309052.5:p.Gln376His
ENST00000312106.5:c.1128G>C ENSP00000309052.5:p.Gln376His
NM_053054.3:c.1128G>C NP_444282.3:p.Gln376His
XR_949785.1:n.1268G>C
XR_949786.1:n.1268G>C
XR_949787.1:n.1268G>C
XR_002957121.1:n.1266G>C
XR_002957122.1:n.1267G>C
XR_949785.2:n.1266G>C
XR_949787.2:n.1267G>C
NM_053054.4:c.1128G>C MANE Select NP_444282.3:p.Gln376His