Canonical Allele Identifier: CA890987937
Gene: KIFAP3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.170026661C>A , CM000663.2:g.170026661C>A GRCh38
NC_000001.10:g.169995802C>A , CM000663.1:g.169995802C>A GRCh37
NC_000001.9:g.168262426C>A NCBI36
NG_012883.2:g.53078G>T
NG_012883.3:g.53078G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361580.7:c.842-2065G>T MANE Select ENSP00000354560.2:n.842-2065G>T
ENST00000361580.6:c.842-2065G>T ENSP00000354560.2:n.842-2065G>T
ENST00000367765.5:c.722-2065G>T ENSP00000356739.1:n.722-2065G>T
ENST00000367767.5:c.710-2065G>T ENSP00000356741.1:n.710-2065G>T
ENST00000474292.1:n.326-2065G>T
ENST00000538366.5:c.608-2065G>T ENSP00000444622.1:n.608-2065G>T
NM_001204514.1:c.608-2065G>T NP_001191443.1:n.608-2065G>T
NM_001204516.1:c.710-2065G>T NP_001191445.1:n.710-2065G>T
NM_001204517.1:c.722-2065G>T NP_001191446.1:n.722-2065G>T
NM_014970.3:c.842-2065G>T NP_055785.2:n.842-2065G>T
XM_005244970.1:c.842-2065G>T XP_005245027.1:n.842-2065G>T
XM_011509307.1:c.722-2065G>T XP_011507609.1:n.722-2065G>T
XM_005244970.2:c.842-2065G>T XP_005245027.1:n.842-2065G>T
XM_011509307.3:c.842-2065G>T XP_011507609.2:n.842-2065G>T
XM_024454186.1:c.887-2065G>T XP_024309954.1:n.887-2065G>T
XM_024454187.1:c.887-2065G>T XP_024309955.1:n.887-2065G>T
NM_014970.4:c.842-2065G>T MANE Select NP_055785.2:n.842-2065G>T
NM_001375830.1:c.842-2065G>T NP_001362759.1:n.842-2065G>T
NM_001375831.1:c.842-2065G>T NP_001362760.1:n.842-2065G>T
NM_001204514.2:c.608-2065G>T NP_001191443.1:n.608-2065G>T
NM_001204516.2:c.710-2065G>T NP_001191445.1:n.710-2065G>T
NM_001204517.2:c.722-2065G>T NP_001191446.1:n.722-2065G>T
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