Canonical Allele Identifier: CA475482762
Gene: CATSPER1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.65792822A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025351A>T , CM000673.2:g.66025351A>T GRCh38
NC_000011.9:g.65792822A>T , CM000673.1:g.65792822A>T GRCh37
NC_000011.8:g.65549398A>T NCBI36
NG_016285.1:g.6167T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000312106.6:c.1029T>A MANE Select ENSP00000309052.5:p.Ala343=
ENST00000312106.5:c.1029T>A ENSP00000309052.5:p.Ala343=
NM_053054.3:c.1029T>A NP_444282.3:p.Ala343=
XR_949785.1:n.1169T>A
XR_949786.1:n.1169T>A
XR_949787.1:n.1169T>A
XR_002957121.1:n.1167T>A
XR_002957122.1:n.1168T>A
XR_949785.2:n.1167T>A
XR_949787.2:n.1168T>A
NM_053054.4:c.1029T>A MANE Select NP_444282.3:p.Ala343=