Canonical Allele Identifier: CA1443500675

Gene: KCNIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.21475383G= , CM000666.2:g.21475383G=	GRCh38
NC_000004.11:g.21477006G= , CM000666.1:g.21477006G=	GRCh37
NC_000004.10:g.21086104G=	NCBI36
NG_052969.1:g.478369C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382152.7:c.61+473188C= MANE Select	ENSP00000371587.2:n.61+473188C=
ENST00000382148.7:c.88+221967C=	ENSP00000371583.3:n.88+221967C=
ENST00000382152.6:c.61+473188C=	ENSP00000371587.2:n.61+473188C=
ENST00000447367.6:c.61+473188C=	ENSP00000399080.2:n.61+473188C=
ENST00000509207.1:c.-24+69007C=	ENSP00000423257.1:n.-24+69007C=
ENST00000515786.2:c.173+287538C=	ENSP00000445321.1:n.173+287538C=
NM_001035003.1:c.88+221967C=	NP_001030175.1:n.88+221967C=
NM_001035004.1:c.-24+69007C=	NP_001030176.1:n.-24+69007C=
NM_025221.5:c.61+473188C=	NP_079497.2:n.61+473188C=
NM_147181.3:c.61+473188C=	NP_671710.1:n.61+473188C=
NM_147182.3:c.-24+287538C=	NP_671711.1:n.-24+287538C=
XM_011513882.1:c.61+473188C=	XP_011512184.1:n.61+473188C=
XM_011513885.1:c.88+221967C=	XP_011512187.1:n.88+221967C=
XM_011513886.1:c.61+473188C=	XP_011512188.1:n.61+473188C=
XM_011513887.1:c.-24+69007C=	XP_011512189.1:n.-24+69007C=
XM_011513888.1:c.-24+287538C=	XP_011512190.1:n.-24+287538C=
XM_011513885.3:c.88+221967C=	XP_011512187.1:n.88+221967C=
XM_011513887.2:c.-24+69007C=	XP_011512189.1:n.-24+69007C=
NM_025221.6:c.61+473188C= MANE Select	NP_079497.2:n.61+473188C=
NM_001035003.2:c.88+221967C=	NP_001030175.1:n.88+221967C=
NM_001035004.2:c.-24+69007C=	NP_001030176.1:n.-24+69007C=
NM_147181.4:c.61+473188C=	NP_671710.1:n.61+473188C=
NM_147182.4:c.-24+287538C=	NP_671711.1:n.-24+287538C=