Canonical Allele Identifier: CA2814503224

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776151_43776152insT , CM000681.2:g.43776151_43776152insT	GRCh38
NC_000019.9:g.44280303_44280304insT , CM000681.1:g.44280303_44280304insT	GRCh37
NC_000019.8:g.48972143_48972144insT	NCBI36
NG_052672.1:g.10988_10989insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+389_255+390insA MANE Select	ENSP00000496939.1:n.255+389_255+390insA
ENST00000262888.7:c.255+389_255+390insA	ENSP00000262888.3:n.255+389_255+390insA
ENST00000599107.1:n.286+389_286+390insA
ENST00000599720.5:c.160-4049_160-4048insA	ENSP00000472513.1:n.160-4049_160-4048insA
ENST00000615047.4:c.70+389_70+390insA	ENSP00000485014.1:n.70+389_70+390insA
NM_002250.2:c.255+389_255+390insA	NP_002241.1:n.255+389_255+390insA
XM_005258882.2:c.160-1533_160-1532insA	XP_005258939.1:n.160-1533_160-1532insA
XM_005258883.2:c.70+389_70+390insA	XP_005258940.1:n.70+389_70+390insA
XM_011526938.1:c.255+389_255+390insA	XP_011525240.1:n.255+389_255+390insA
XR_935823.1:n.1533+389_1533+390insA
XR_002958313.1:n.1533+389_1533+390insA
NM_002250.3:c.255+389_255+390insA MANE Select	NP_002241.1:n.255+389_255+390insA