Canonical Allele Identifier: CA1979517819
Gene: CATSPER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025442T= , CM000673.2:g.66025442T= GRCh38
NC_000011.9:g.65792913T= , CM000673.1:g.65792913T= GRCh37
NC_000011.8:g.65549489T= NCBI36
NG_016285.1:g.6076A=

Transcript Alleles

HGVS Amino-acid change
ENST00000312106.6:c.938A= MANE Select ENSP00000309052.5:p.Tyr313=
ENST00000312106.5:c.938A= ENSP00000309052.5:p.Tyr313=
NM_053054.3:c.938A= NP_444282.3:p.Tyr313=
XR_949785.1:n.1078A=
XR_949786.1:n.1078A=
XR_949787.1:n.1078A=
XR_002957121.1:n.1076A=
XR_002957122.1:n.1077A=
XR_949785.2:n.1076A=
XR_949787.2:n.1077A=
NM_053054.4:c.938A= MANE Select NP_444282.3:p.Tyr313=