Canonical Allele Identifier: CA381338369
Gene: CATSPER1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025443A>G , CM000673.2:g.66025443A>G GRCh38
NC_000011.9:g.65792914A>G , CM000673.1:g.65792914A>G GRCh37
NC_000011.8:g.65549490A>G NCBI36
NG_016285.1:g.6075T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000312106.6:c.937T>C MANE Select ENSP00000309052.5:p.Tyr313His
ENST00000312106.5:c.937T>C ENSP00000309052.5:p.Tyr313His
NM_053054.3:c.937T>C NP_444282.3:p.Tyr313His
XR_949785.1:n.1077T>C
XR_949786.1:n.1077T>C
XR_949787.1:n.1077T>C
XR_002957121.1:n.1075T>C
XR_002957122.1:n.1076T>C
XR_949785.2:n.1075T>C
XR_949787.2:n.1076T>C
NM_053054.4:c.937T>C MANE Select NP_444282.3:p.Tyr313His