Canonical Allele Identifier: CA2337655757

Gene: KCNN4

Linked Data

• dbSNP Id: rs1969807852

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776479_43776480del , CM000681.2:g.43776479_43776480del	GRCh38
NC_000019.9:g.44280631_44280632del , CM000681.1:g.44280631_44280632del	GRCh37
NC_000019.8:g.48972471_48972472del	NCBI36
NG_052672.1:g.10663_10664del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+64_255+65del MANE Select	ENSP00000496939.1:n.255+64_255+65del
ENST00000262888.7:c.255+64_255+65del	ENSP00000262888.3:n.255+64_255+65del
ENST00000599107.1:n.286+64_286+65del
ENST00000599720.5:c.159+4226_159+4227del	ENSP00000472513.1:n.159+4226_159+4227del
ENST00000615047.4:c.70+64_70+65del	ENSP00000485014.1:n.70+64_70+65del
NM_002250.2:c.255+64_255+65del	NP_002241.1:n.255+64_255+65del
XM_005258882.2:c.160-1858_160-1857del	XP_005258939.1:n.160-1858_160-1857del
XM_005258883.2:c.70+64_70+65del	XP_005258940.1:n.70+64_70+65del
XM_011526938.1:c.255+64_255+65del	XP_011525240.1:n.255+64_255+65del
XR_935823.1:n.1533+64_1533+65del
XR_002958313.1:n.1533+64_1533+65del
NM_002250.3:c.255+64_255+65del MANE Select	NP_002241.1:n.255+64_255+65del