Canonical Allele Identifier: CA398352444

Gene: NEK8

Linked Data

• MyVariant Identifiers: chr17:g.27065703A>T (hg19) ; chr17:g.28738685A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28738685A>T , CM000679.2:g.28738685A>T	GRCh38
NC_000017.10:g.27065703A>T , CM000679.1:g.27065703A>T	GRCh37
NC_000017.9:g.24089830A>T	NCBI36
NG_012263.1:g.14872A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268766.11:c.1237A>T MANE Select	ENSP00000268766.6:p.Met413Leu
ENST00000268766.10:c.1237A>T	ENSP00000268766.6:p.Met413Leu
ENST00000543014.1:c.*14A>T	ENSP00000465859.1:n.*14A>T
NM_178170.2:c.1237A>T	NP_835464.1:p.Met413Leu
XM_011524638.1:c.1348A>T	XP_011522940.1:p.Met450Leu
XM_011524639.1:c.1321A>T	XP_011522941.1:p.Met441Leu
XM_011524640.1:c.1309A>T	XP_011522942.1:p.Met437Leu
XM_011524641.1:c.1204A>T	XP_011522943.1:p.Met402Leu
XM_011524642.1:c.1204A>T	XP_011522944.1:p.Met402Leu
XM_011524643.1:c.1204A>T	XP_011522945.1:p.Met402Leu
XM_011524644.1:c.1027A>T	XP_011522946.1:p.Met343Leu
XM_011524645.1:c.*10A>T	XP_011522947.1:n.*10A>T
XR_934448.1:n.1521A>T
NM_178170.3:c.1237A>T MANE Select	NP_835464.1:p.Met413Leu
XM_011524638.3:c.1348A>T	XP_011522940.1:p.Met450Leu
XM_011524640.3:c.1309A>T	XP_011522942.1:p.Met437Leu
XM_017024499.2:c.1276A>T	XP_016879988.1:p.Met426Leu
XM_017024500.2:c.1159A>T	XP_016879989.1:p.Met387Leu
XM_017024501.1:c.*10A>T	XP_016879990.1:n.*10A>T
XR_001752497.2:n.1476A>T