Canonical Allele Identifier: CA475482799
Gene: CATSPER1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.65792873A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025402A>G , CM000673.2:g.66025402A>G GRCh38
NC_000011.9:g.65792873A>G , CM000673.1:g.65792873A>G GRCh37
NC_000011.8:g.65549449A>G NCBI36
NG_016285.1:g.6116T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000312106.6:c.978T>C MANE Select ENSP00000309052.5:p.Ser326=
ENST00000312106.5:c.978T>C ENSP00000309052.5:p.Ser326=
NM_053054.3:c.978T>C NP_444282.3:p.Ser326=
XR_949785.1:n.1118T>C
XR_949786.1:n.1118T>C
XR_949787.1:n.1118T>C
XR_002957121.1:n.1116T>C
XR_002957122.1:n.1117T>C
XR_949785.2:n.1116T>C
XR_949787.2:n.1117T>C
NM_053054.4:c.978T>C MANE Select NP_444282.3:p.Ser326=