Canonical Allele Identifier: CA2581410894

Gene: KCNIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.21569464T>G , CM000666.2:g.21569464T>G	GRCh38
NC_000004.11:g.21571087T>G , CM000666.1:g.21571087T>G	GRCh37
NC_000004.10:g.21180185T>G	NCBI36
NG_052969.1:g.384288A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382152.7:c.61+379107A>C MANE Select	ENSP00000371587.2:n.61+379107A>C
ENST00000382148.7:c.88+127886A>C	ENSP00000371583.3:n.88+127886A>C
ENST00000382152.6:c.61+379107A>C	ENSP00000371587.2:n.61+379107A>C
ENST00000447367.6:c.61+379107A>C	ENSP00000399080.2:n.61+379107A>C
ENST00000515786.2:c.173+193457A>C	ENSP00000445321.1:n.173+193457A>C
NM_001035003.1:c.88+127886A>C	NP_001030175.1:n.88+127886A>C
NM_025221.5:c.61+379107A>C	NP_079497.2:n.61+379107A>C
NM_147181.3:c.61+379107A>C	NP_671710.1:n.61+379107A>C
NM_147182.3:c.-24+193457A>C	NP_671711.1:n.-24+193457A>C
XM_011513882.1:c.61+379107A>C	XP_011512184.1:n.61+379107A>C
XM_011513885.1:c.88+127886A>C	XP_011512187.1:n.88+127886A>C
XM_011513886.1:c.61+379107A>C	XP_011512188.1:n.61+379107A>C
XM_011513888.1:c.-24+193457A>C	XP_011512190.1:n.-24+193457A>C
XM_011513885.3:c.88+127886A>C	XP_011512187.1:n.88+127886A>C
NM_025221.6:c.61+379107A>C MANE Select	NP_079497.2:n.61+379107A>C
NM_001035003.2:c.88+127886A>C	NP_001030175.1:n.88+127886A>C
NM_147181.4:c.61+379107A>C	NP_671710.1:n.61+379107A>C
NM_147182.4:c.-24+193457A>C	NP_671711.1:n.-24+193457A>C