Canonical Allele Identifier: CA2340843093

Gene: KCNC3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50323609G= , CM000681.2:g.50323609G=	GRCh38
NC_000019.9:g.50826866G= , CM000681.1:g.50826866G=	GRCh37
NC_000019.8:g.55518678G=	NCBI36
NG_008134.2:g.10769C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004977.3:c.1344C= MANE Select	NP_004968.2:p.Phe448=
ENST00000477616.2:c.1344C= MANE Select	ENSP00000434241.1:p.Phe448=
NM_001372305.1:c.1116C=	NP_001359234.1:p.Phe372=
NM_004977.2:c.1344C=	NP_004968.2:p.Phe448=
NR_110912.1:n.48-2825C=
NR_110912.2:n.69-2825C=
ENST00000376959.6:c.1344C=	ENSP00000366158.2:p.Phe448=
ENST00000474951.1:c.-74-2825C=	ENSP00000432438.1:n.-74-2825C=
ENST00000477616.1:c.1344C=	ENSP00000434241.1:p.Phe448=
ENST00000670667.1:c.1344C=	ENSP00000499301.1:p.Phe448=
XM_006723203.2:c.1344C=	XP_006723266.1:p.Phe448=
XM_011526925.1:c.1344C=	XP_011525227.1:p.Phe448=
XM_011526926.1:c.1344C=	XP_011525228.1:p.Phe448=
XM_011526927.1:c.1344C=	XP_011525229.1:p.Phe448=
XM_011526928.1:c.1344C=	XP_011525230.1:p.Phe448=