Canonical Allele Identifier: CA475482751
Gene: CATSPER1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.65792810T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025339T>G , CM000673.2:g.66025339T>G GRCh38
NC_000011.9:g.65792810T>G , CM000673.1:g.65792810T>G GRCh37
NC_000011.8:g.65549386T>G NCBI36
NG_016285.1:g.6179A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000312106.6:c.1041A>C MANE Select ENSP00000309052.5:p.Gly347=
ENST00000312106.5:c.1041A>C ENSP00000309052.5:p.Gly347=
NM_053054.3:c.1041A>C NP_444282.3:p.Gly347=
XR_949785.1:n.1181A>C
XR_949786.1:n.1181A>C
XR_949787.1:n.1181A>C
XR_002957121.1:n.1179A>C
XR_002957122.1:n.1180A>C
XR_949785.2:n.1179A>C
XR_949787.2:n.1180A>C
NM_053054.4:c.1041A>C MANE Select NP_444282.3:p.Gly347=