Canonical Allele Identifier: CA381336352
Gene: CATSPER1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025251T>C , CM000673.2:g.66025251T>C GRCh38
NC_000011.9:g.65792722T>C , CM000673.1:g.65792722T>C GRCh37
NC_000011.8:g.65549298T>C NCBI36
NG_016285.1:g.6267A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312106.6:c.1129A>G MANE Select ENSP00000309052.5:p.Met377Val
ENST00000312106.5:c.1129A>G ENSP00000309052.5:p.Met377Val
NM_053054.3:c.1129A>G NP_444282.3:p.Met377Val
XR_949785.1:n.1269A>G
XR_949786.1:n.1269A>G
XR_949787.1:n.1269A>G
XR_002957121.1:n.1267A>G
XR_002957122.1:n.1268A>G
XR_949785.2:n.1267A>G
XR_949787.2:n.1268A>G
NM_053054.4:c.1129A>G MANE Select NP_444282.3:p.Met377Val