Canonical Allele Identifier: CA381338421
Gene: CATSPER1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025448G>C , CM000673.2:g.66025448G>C GRCh38
NC_000011.9:g.65792919G>C , CM000673.1:g.65792919G>C GRCh37
NC_000011.8:g.65549495G>C NCBI36
NG_016285.1:g.6070C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000312106.6:c.932C>G MANE Select ENSP00000309052.5:p.Ser311Cys
ENST00000312106.5:c.932C>G ENSP00000309052.5:p.Ser311Cys
NM_053054.3:c.932C>G NP_444282.3:p.Ser311Cys
XR_949785.1:n.1072C>G
XR_949786.1:n.1072C>G
XR_949787.1:n.1072C>G
XR_002957121.1:n.1070C>G
XR_002957122.1:n.1071C>G
XR_949785.2:n.1070C>G
XR_949787.2:n.1071C>G
NM_053054.4:c.932C>G MANE Select NP_444282.3:p.Ser311Cys