Canonical Allele Identifier: CA381337089
Gene: CATSPER1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66025340C>A , CM000673.2:g.66025340C>A GRCh38
NC_000011.9:g.65792811C>A , CM000673.1:g.65792811C>A GRCh37
NC_000011.8:g.65549387C>A NCBI36
NG_016285.1:g.6178G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000312106.6:c.1040G>T MANE Select ENSP00000309052.5:p.Gly347Val
ENST00000312106.5:c.1040G>T ENSP00000309052.5:p.Gly347Val
NM_053054.3:c.1040G>T NP_444282.3:p.Gly347Val
XR_949785.1:n.1180G>T
XR_949786.1:n.1180G>T
XR_949787.1:n.1180G>T
XR_002957121.1:n.1178G>T
XR_002957122.1:n.1179G>T
XR_949785.2:n.1178G>T
XR_949787.2:n.1179G>T
NM_053054.4:c.1040G>T MANE Select NP_444282.3:p.Gly347Val