Canonical Allele Identifier: CA1600414973

Gene: KCNIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.170523411T= , CM000667.2:g.170523411T=	GRCh38
NC_000005.9:g.169950415T= , CM000667.1:g.169950415T=	GRCh37
NC_000005.8:g.169882993T=	NCBI36
NG_011538.1:g.174535T=
NG_011538.2:g.174535T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328939.9:c.61+18778T= MANE Select	ENSP00000329686.4:n.61+18778T=
ENST00000328939.8:c.61+18778T=	ENSP00000329686.4:n.61+18778T=
ENST00000377360.8:c.88+169447T=	ENSP00000366577.4:n.88+169447T=
ENST00000390656.8:c.-165+18778T=	ENSP00000375071.5:n.-165+18778T=
ENST00000411494.5:c.61+18778T=	ENSP00000395323.1:n.61+18778T=
ENST00000434108.5:c.61+18778T=	ENSP00000414886.1:n.61+18778T=
ENST00000520740.5:c.-186+18778T=	ENSP00000431102.1:n.-186+18778T=
NM_001034837.2:c.61+18778T=	NP_001030009.1:n.61+18778T=
NM_001034838.2:c.88+169447T=	NP_001030010.1:n.88+169447T=
NM_001278339.1:c.61+18778T=	NP_001265268.1:n.61+18778T=
NM_001278340.1:c.-186+18778T=	NP_001265269.1:n.-186+18778T=
NM_014592.3:c.61+18778T=	NP_055407.1:n.61+18778T=
XM_006714861.1:c.136+40216T=	XP_006714924.1:n.136+40216T=
XM_011534539.1:c.241+37435T=	XP_011532841.1:n.241+37435T=
XM_017009407.1:c.88+169447T=	XP_016864896.1:n.88+169447T=
NM_001034837.3:c.61+18778T=	NP_001030009.1:n.61+18778T=
NM_001034838.3:c.88+169447T=	NP_001030010.1:n.88+169447T=
NM_001278339.2:c.61+18778T=	NP_001265268.1:n.61+18778T=
NM_001278340.2:c.-186+18778T=	NP_001265269.1:n.-186+18778T=
NM_014592.4:c.61+18778T= MANE Select	NP_055407.1:n.61+18778T=