Canonical Allele Identifier: CA9594239

Gene: KCNC3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50323531G>A , CM000681.2:g.50323531G>A	GRCh38
NC_000019.9:g.50826788G>A , CM000681.1:g.50826788G>A	GRCh37
NC_000019.8:g.55518600G>A	NCBI36
NG_008134.2:g.10847C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477616.2:c.1422C>T MANE Select	ENSP00000434241.1:p.Ala474=
ENST00000670667.1:c.1422C>T	ENSP00000499301.1:p.Ala474=
ENST00000376959.6:c.1422C>T	ENSP00000366158.2:p.Ala474=
ENST00000474951.1:c.-74-2747C>T	ENSP00000432438.1:n.-74-2747C>T
ENST00000477616.1:c.1422C>T	ENSP00000434241.1:p.Ala474=
NM_004977.2:c.1422C>T	NP_004968.2:p.Ala474=
NR_110912.1:n.48-2747C>T
XM_006723203.2:c.1422C>T	XP_006723266.1:p.Ala474=
XM_011526925.1:c.1422C>T	XP_011525227.1:p.Ala474=
XM_011526926.1:c.1422C>T	XP_011525228.1:p.Ala474=
XM_011526927.1:c.1422C>T	XP_011525229.1:p.Ala474=
XM_011526928.1:c.1422C>T	XP_011525230.1:p.Ala474=
NM_001372305.1:c.1194C>T	NP_001359234.1:p.Ala398=
NM_004977.3:c.1422C>T MANE Select	NP_004968.2:p.Ala474=
NR_110912.2:n.69-2747C>T