Canonical Allele Identifier: CA2337655699

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776350A= , CM000681.2:g.43776350A=	GRCh38
NC_000019.9:g.44280502A= , CM000681.1:g.44280502A=	GRCh37
NC_000019.8:g.48972342A=	NCBI36
NG_052672.1:g.10790T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+191T= MANE Select	ENSP00000496939.1:n.255+191T=
ENST00000262888.7:c.255+191T=	ENSP00000262888.3:n.255+191T=
ENST00000599107.1:n.286+191T=
ENST00000599720.5:c.160-4247T=	ENSP00000472513.1:n.160-4247T=
ENST00000615047.4:c.70+191T=	ENSP00000485014.1:n.70+191T=
NM_002250.2:c.255+191T=	NP_002241.1:n.255+191T=
XM_005258882.2:c.160-1731T=	XP_005258939.1:n.160-1731T=
XM_005258883.2:c.70+191T=	XP_005258940.1:n.70+191T=
XM_011526938.1:c.255+191T=	XP_011525240.1:n.255+191T=
XR_935823.1:n.1533+191T=
XR_002958313.1:n.1533+191T=
NM_002250.3:c.255+191T= MANE Select	NP_002241.1:n.255+191T=