Canonical Allele Identifier: CA1443379956

Gene: KCNIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.21204867T= , CM000666.2:g.21204867T=	GRCh38
NC_000004.11:g.21206490T= , CM000666.1:g.21206490T=	GRCh37
NC_000004.10:g.20815588T=	NCBI36
NG_052969.1:g.748885A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382152.7:c.62-322158A= MANE Select	ENSP00000371587.2:n.62-322158A=
ENST00000382148.7:c.89-354200A=	ENSP00000371583.3:n.89-354200A=
ENST00000382150.8:c.100+98940A=	ENSP00000371585.4:n.100+98940A=
ENST00000382152.6:c.62-322158A=	ENSP00000371587.2:n.62-322158A=
ENST00000447367.6:c.62-354200A=	ENSP00000399080.2:n.62-354200A=
ENST00000509207.1:c.-24+339523A=	ENSP00000423257.1:n.-24+339523A=
ENST00000515786.2:c.174-354200A=	ENSP00000445321.1:n.174-354200A=
NM_001035003.1:c.89-354200A=	NP_001030175.1:n.89-354200A=
NM_001035004.1:c.-24+339523A=	NP_001030176.1:n.-24+339523A=
NM_025221.5:c.62-322158A=	NP_079497.2:n.62-322158A=
NM_147181.3:c.62-354200A=	NP_671710.1:n.62-354200A=
NM_147182.3:c.-23-354200A=	NP_671711.1:n.-23-354200A=
NM_147183.3:c.100+98940A=	NP_671712.1:n.100+98940A=
XM_011513882.1:c.62-322158A=	XP_011512184.1:n.62-322158A=
XM_011513884.1:c.100+98940A=	XP_011512186.1:n.100+98940A=
XM_011513885.1:c.89-354200A=	XP_011512187.1:n.89-354200A=
XM_011513886.1:c.62-354200A=	XP_011512188.1:n.62-354200A=
XM_011513887.1:c.-24+339523A=	XP_011512189.1:n.-24+339523A=
XM_011513888.1:c.-23-354200A=	XP_011512190.1:n.-23-354200A=
XM_011513885.3:c.89-354200A=	XP_011512187.1:n.89-354200A=
XM_011513887.2:c.-24+339523A=	XP_011512189.1:n.-24+339523A=
NM_025221.6:c.62-322158A= MANE Select	NP_079497.2:n.62-322158A=
NM_001035003.2:c.89-354200A=	NP_001030175.1:n.89-354200A=
NM_001035004.2:c.-24+339523A=	NP_001030176.1:n.-24+339523A=
NM_147181.4:c.62-354200A=	NP_671710.1:n.62-354200A=
NM_147182.4:c.-23-354200A=	NP_671711.1:n.-23-354200A=