Canonical Allele Identifier: CA1443500700

Gene: KCNIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.21475402A= , CM000666.2:g.21475402A=	GRCh38
NC_000004.11:g.21477025A= , CM000666.1:g.21477025A=	GRCh37
NC_000004.10:g.21086123A=	NCBI36
NG_052969.1:g.478350T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382152.7:c.61+473169T= MANE Select	ENSP00000371587.2:n.61+473169T=
ENST00000382148.7:c.88+221948T=	ENSP00000371583.3:n.88+221948T=
ENST00000382152.6:c.61+473169T=	ENSP00000371587.2:n.61+473169T=
ENST00000447367.6:c.61+473169T=	ENSP00000399080.2:n.61+473169T=
ENST00000509207.1:c.-24+68988T=	ENSP00000423257.1:n.-24+68988T=
ENST00000515786.2:c.173+287519T=	ENSP00000445321.1:n.173+287519T=
NM_001035003.1:c.88+221948T=	NP_001030175.1:n.88+221948T=
NM_001035004.1:c.-24+68988T=	NP_001030176.1:n.-24+68988T=
NM_025221.5:c.61+473169T=	NP_079497.2:n.61+473169T=
NM_147181.3:c.61+473169T=	NP_671710.1:n.61+473169T=
NM_147182.3:c.-24+287519T=	NP_671711.1:n.-24+287519T=
XM_011513882.1:c.61+473169T=	XP_011512184.1:n.61+473169T=
XM_011513885.1:c.88+221948T=	XP_011512187.1:n.88+221948T=
XM_011513886.1:c.61+473169T=	XP_011512188.1:n.61+473169T=
XM_011513887.1:c.-24+68988T=	XP_011512189.1:n.-24+68988T=
XM_011513888.1:c.-24+287519T=	XP_011512190.1:n.-24+287519T=
XM_011513885.3:c.88+221948T=	XP_011512187.1:n.88+221948T=
XM_011513887.2:c.-24+68988T=	XP_011512189.1:n.-24+68988T=
NM_025221.6:c.61+473169T= MANE Select	NP_079497.2:n.61+473169T=
NM_001035003.2:c.88+221948T=	NP_001030175.1:n.88+221948T=
NM_001035004.2:c.-24+68988T=	NP_001030176.1:n.-24+68988T=
NM_147181.4:c.61+473169T=	NP_671710.1:n.61+473169T=
NM_147182.4:c.-24+287519T=	NP_671711.1:n.-24+287519T=