Canonical Allele Identifier: CA1141068302
Gene: CATSPER4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26194665G= , CM000663.2:g.26194665G= GRCh38
NC_000001.10:g.26521156G= , CM000663.1:g.26521156G= GRCh37
NC_000001.9:g.26393743G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000456354.7:c.459+777G= MANE Select ENSP00000390423.3:n.459+777G=
ENST00000338855.6:c.459+777G= ENSP00000341006.2:n.459+777G=
ENST00000456354.6:c.459+777G= ENSP00000390423.2:n.459+777G=
ENST00000518899.5:c.459+777G= ENSP00000429464.1:n.459+777G=
ENST00000611853.1:c.426+777G= ENSP00000477936.1:n.426+777G=
NM_198137.1:c.459+777G= NP_937770.1:n.459+777G=
XM_011541432.1:c.459+777G= XP_011539734.1:n.459+777G=
XM_011541433.1:c.459+777G= XP_011539735.1:n.459+777G=
XM_011541432.3:c.459+777G= XP_011539734.1:n.459+777G=
XM_011541433.2:c.459+777G= XP_011539735.1:n.459+777G=
NM_198137.2:c.459+777G= MANE Select NP_937770.1:n.459+777G=