Canonical Allele Identifier: CA1443500588

Gene: KCNIP4

Linked Data

• dbSNP Id: rs1730858217

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.21475299C>T , CM000666.2:g.21475299C>T	GRCh38
NC_000004.11:g.21476922C>T , CM000666.1:g.21476922C>T	GRCh37
NC_000004.10:g.21086020C>T	NCBI36
NG_052969.1:g.478453G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382152.7:c.61+473272G>A MANE Select	ENSP00000371587.2:n.61+473272G>A
ENST00000382148.7:c.88+222051G>A	ENSP00000371583.3:n.88+222051G>A
ENST00000382152.6:c.61+473272G>A	ENSP00000371587.2:n.61+473272G>A
ENST00000447367.6:c.61+473272G>A	ENSP00000399080.2:n.61+473272G>A
ENST00000509207.1:c.-24+69091G>A	ENSP00000423257.1:n.-24+69091G>A
ENST00000515786.2:c.173+287622G>A	ENSP00000445321.1:n.173+287622G>A
NM_001035003.1:c.88+222051G>A	NP_001030175.1:n.88+222051G>A
NM_001035004.1:c.-24+69091G>A	NP_001030176.1:n.-24+69091G>A
NM_025221.5:c.61+473272G>A	NP_079497.2:n.61+473272G>A
NM_147181.3:c.61+473272G>A	NP_671710.1:n.61+473272G>A
NM_147182.3:c.-24+287622G>A	NP_671711.1:n.-24+287622G>A
XM_011513882.1:c.61+473272G>A	XP_011512184.1:n.61+473272G>A
XM_011513885.1:c.88+222051G>A	XP_011512187.1:n.88+222051G>A
XM_011513886.1:c.61+473272G>A	XP_011512188.1:n.61+473272G>A
XM_011513887.1:c.-24+69091G>A	XP_011512189.1:n.-24+69091G>A
XM_011513888.1:c.-24+287622G>A	XP_011512190.1:n.-24+287622G>A
XM_011513885.3:c.88+222051G>A	XP_011512187.1:n.88+222051G>A
XM_011513887.2:c.-24+69091G>A	XP_011512189.1:n.-24+69091G>A
NM_025221.6:c.61+473272G>A MANE Select	NP_079497.2:n.61+473272G>A
NM_001035003.2:c.88+222051G>A	NP_001030175.1:n.88+222051G>A
NM_001035004.2:c.-24+69091G>A	NP_001030176.1:n.-24+69091G>A
NM_147181.4:c.61+473272G>A	NP_671710.1:n.61+473272G>A
NM_147182.4:c.-24+287622G>A	NP_671711.1:n.-24+287622G>A