Canonical Allele Identifier: CA6510771
Community Standard Title: NM_001173464.2(KIF21A):c.2492C>T (p.Thr831Met)
Gene: KIF21A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39333103G>A , CM000674.2:g.39333103G>A GRCh38
NC_000012.11:g.39726905G>A , CM000674.1:g.39726905G>A GRCh37
NC_000012.10:g.38013172G>A NCBI36
NG_017067.1:g.115288C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001173464.2:c.2492C>T MANE Select NP_001166935.1:p.Thr831Met
ENST00000361418.10:c.2492C>T MANE Select ENSP00000354878.5:p.Thr831Met
NM_001173463.1:c.2453C>T NP_001166934.1:p.Thr818Met
NM_001173463.2:c.2453C>T NP_001166934.1:p.Thr818Met
NM_001173464.1:c.2492C>T NP_001166935.1:p.Thr831Met
NM_001173465.1:c.2384C>T NP_001166936.1:p.Thr795Met
NM_001173465.2:c.2384C>T NP_001166936.1:p.Thr795Met
NM_001378439.1:c.2492C>T NP_001365368.1:p.Thr831Met
NM_001378440.1:c.2492C>T NP_001365369.1:p.Thr831Met
NM_001378441.1:c.2453C>T NP_001365370.1:p.Thr818Met
NM_017641.3:c.2453C>T NP_060111.2:p.Thr818Met
NM_017641.4:c.2453C>T NP_060111.2:p.Thr818Met
ENST00000361418.9:c.2492C>T ENSP00000354878.5:p.Thr831Met
ENST00000361961.7:c.2453C>T ENSP00000354851.3:p.Thr818Met
ENST00000541463.6:c.2384C>T ENSP00000438075.2:p.Thr795Met
ENST00000544797.6:c.2453C>T ENSP00000445606.2:p.Thr818Met
ENST00000546817.1:n.520C>T
ENST00000547108.5:c.265C>T
ENST00000552961.5:c.535C>T
ENST00000636569.1:c.2426C>T ENSP00000490369.1:p.Thr809Met
XM_005269007.1:c.2492C>T XP_005269064.1:p.Thr831Met
XM_005269007.3:c.2492C>T XP_005269064.1:p.Thr831Met
XM_005269008.1:c.2492C>T XP_005269065.1:p.Thr831Met
XM_005269008.3:c.2492C>T XP_005269065.1:p.Thr831Met
XM_005269009.1:c.2492C>T XP_005269066.1:p.Thr831Met
XM_005269009.3:c.2492C>T XP_005269066.1:p.Thr831Met
XM_005269010.1:c.2453C>T XP_005269067.1:p.Thr818Met
XM_005269010.3:c.2453C>T XP_005269067.1:p.Thr818Met
XM_005269011.1:c.2492C>T XP_005269068.1:p.Thr831Met
XM_005269011.3:c.2492C>T XP_005269068.1:p.Thr831Met
XM_005269012.1:c.2492C>T XP_005269069.1:p.Thr831Met
XM_005269012.3:c.2492C>T XP_005269069.1:p.Thr831Met
XM_005269013.1:c.2492C>T XP_005269070.1:p.Thr831Met
XM_005269013.3:c.2492C>T XP_005269070.1:p.Thr831Met
XM_005269014.1:c.2492C>T XP_005269071.1:p.Thr831Met
XM_005269014.3:c.2492C>T XP_005269071.1:p.Thr831Met
XM_006719493.1:c.2453C>T XP_006719556.1:p.Thr818Met
XM_006719493.3:c.2453C>T XP_006719556.1:p.Thr818Met
XM_006719494.1:c.2492C>T XP_006719557.1:p.Thr831Met
XM_006719494.3:c.2492C>T XP_006719557.1:p.Thr831Met
XM_006719496.1:c.2453C>T XP_006719559.1:p.Thr818Met
XM_011538556.1:c.2423C>T XP_011536858.1:p.Thr808Met
XM_011538556.3:c.2423C>T XP_011536858.1:p.Thr808Met
XM_017019607.2:c.2453C>T XP_016875096.1:p.Thr818Met
XM_017019608.2:c.2453C>T XP_016875097.1:p.Thr818Met
XM_017019609.2:c.2453C>T XP_016875098.1:p.Thr818Met
XM_017019610.2:c.2492C>T XP_016875099.1:p.Thr831Met
XM_017019611.2:c.2453C>T XP_016875100.1:p.Thr818Met
XR_429108.1:n.2824C>T