Canonical Allele Identifier: CA1164545361
Gene: KCNQ4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40819472G= , CM000663.2:g.40819472G= GRCh38
NC_000001.10:g.41285144G= , CM000663.1:g.41285144G= GRCh37
NC_000001.9:g.41057731G= NCBI36
NG_008139.1:g.40461G=
NG_008139.2:g.40461G=
NG_008139.3:g.40686G=

Transcript Alleles

HGVS Amino-acid change
ENST00000347132.10:c.834G= MANE Select ENSP00000262916.6:p.Thr278=
ENST00000347132.9:c.834G= ENSP00000262916.6:p.Thr278=
ENST00000443478.3:c.520G=
ENST00000506017.1:n.153G=
ENST00000509682.6:c.834G= ENSP00000423756.2:p.Thr278=
NM_004700.3:c.834G= NP_004691.2:p.Thr278=
NM_172163.2:c.834G= NP_751895.1:p.Thr278=
XM_011542417.1:c.834G= XP_011540719.1:p.Thr278=
XM_011542418.1:c.834G= XP_011540720.1:p.Thr278=
XM_011542419.1:c.834G= XP_011540721.1:p.Thr278=
XM_011542420.1:c.834G= XP_011540722.1:p.Thr278=
XR_946798.1:n.840G=
XR_946799.1:n.840G=
XR_946800.1:n.840G=
XM_017002792.1:c.-184G= XP_016858281.1:n.-184G=
NM_004700.4:c.834G= MANE Select NP_004691.2:p.Thr278=
NM_172163.3:c.834G= NP_751895.1:p.Thr278=