Canonical Allele Identifier: CA475482847
Gene: CATSPER1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.65792918G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025447G>T , CM000673.2:g.66025447G>T GRCh38
NC_000011.9:g.65792918G>T , CM000673.1:g.65792918G>T GRCh37
NC_000011.8:g.65549494G>T NCBI36
NG_016285.1:g.6071C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000312106.6:c.933C>A MANE Select ENSP00000309052.5:p.Ser311=
ENST00000312106.5:c.933C>A ENSP00000309052.5:p.Ser311=
NM_053054.3:c.933C>A NP_444282.3:p.Ser311=
XR_949785.1:n.1073C>A
XR_949786.1:n.1073C>A
XR_949787.1:n.1073C>A
XR_002957121.1:n.1071C>A
XR_002957122.1:n.1072C>A
XR_949785.2:n.1071C>A
XR_949787.2:n.1072C>A
NM_053054.4:c.933C>A MANE Select NP_444282.3:p.Ser311=