Canonical Allele Identifier: CA384386878

Gene: KIF21A

Linked Data

• gnomAD v4: 12-39309613-T-C
• MyVariant Identifiers: chr12:g.39703415T>C (hg19) ; chr12:g.39309613T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309613T>C , CM000674.2:g.39309613T>C	GRCh38
NC_000012.11:g.39703415T>C , CM000674.1:g.39703415T>C	GRCh37
NC_000012.10:g.37989682T>C	NCBI36
NG_017067.1:g.138778A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4250A>G MANE Select	ENSP00000354878.5:p.Asp1417Gly
ENST00000636569.1:c.4187A>G	ENSP00000490369.1:p.Asp1396Gly
ENST00000361418.9:c.4250A>G	ENSP00000354878.5:p.Asp1417Gly
ENST00000361961.7:c.4211A>G	ENSP00000354851.3:p.Asp1404Gly
ENST00000541463.6:c.4091A>G	ENSP00000438075.2:p.Asp1364Gly
ENST00000544797.6:c.4139A>G	ENSP00000445606.2:p.Asp1380Gly
ENST00000547733.1:n.1564A>G
ENST00000551264.5:c.1193A>G	ENSP00000448792.1:p.Asp398Gly
ENST00000552961.5:c.2152A>G
NM_001173463.1:c.4139A>G	NP_001166934.1:p.Asp1380Gly
NM_001173464.1:c.4250A>G	NP_001166935.1:p.Asp1417Gly
NM_001173465.1:c.4091A>G	NP_001166936.1:p.Asp1364Gly
NM_017641.3:c.4211A>G	NP_060111.2:p.Asp1404Gly
XM_005269007.1:c.4253A>G	XP_005269064.1:p.Asp1418Gly
XM_005269008.1:c.4238A>G	XP_005269065.1:p.Asp1413Gly
XM_005269009.1:c.4232A>G	XP_005269066.1:p.Asp1411Gly
XM_005269010.1:c.4214A>G	XP_005269067.1:p.Asp1405Gly
XM_005269011.1:c.4199A>G	XP_005269068.1:p.Asp1400Gly
XM_005269012.1:c.4124A>G	XP_005269069.1:p.Asp1375Gly
XM_005269013.1:c.4109A>G	XP_005269070.1:p.Asp1370Gly
XM_005269014.1:c.4070A>G	XP_005269071.1:p.Asp1357Gly
XM_006719493.1:c.4193A>G	XP_006719556.1:p.Asp1398Gly
XM_006719494.1:c.4121A>G	XP_006719557.1:p.Asp1374Gly
XM_006719496.1:c.4178A>G	XP_006719559.1:p.Asp1393Gly
XM_011538556.1:c.4184A>G	XP_011536858.1:p.Asp1395Gly
XM_005269007.3:c.4253A>G	XP_005269064.1:p.Asp1418Gly
XM_005269008.3:c.4238A>G	XP_005269065.1:p.Asp1413Gly
XM_005269009.3:c.4232A>G	XP_005269066.1:p.Asp1411Gly
XM_005269010.3:c.4214A>G	XP_005269067.1:p.Asp1405Gly
XM_005269011.3:c.4199A>G	XP_005269068.1:p.Asp1400Gly
XM_005269012.3:c.4124A>G	XP_005269069.1:p.Asp1375Gly
XM_005269013.3:c.4109A>G	XP_005269070.1:p.Asp1370Gly
XM_005269014.3:c.4070A>G	XP_005269071.1:p.Asp1357Gly
XM_006719493.3:c.4193A>G	XP_006719556.1:p.Asp1398Gly
XM_006719494.3:c.4121A>G	XP_006719557.1:p.Asp1374Gly
XM_011538556.3:c.4184A>G	XP_011536858.1:p.Asp1395Gly
XM_017019607.2:c.4199A>G	XP_016875096.1:p.Asp1400Gly
XM_017019608.2:c.4160A>G	XP_016875097.1:p.Asp1387Gly
XM_017019609.2:c.4049A>G	XP_016875098.1:p.Asp1350Gly
XM_017019610.2:c.4049A>G	XP_016875099.1:p.Asp1350Gly
XM_017019611.2:c.4031A>G	XP_016875100.1:p.Asp1344Gly
NM_001173463.2:c.4139A>G	NP_001166934.1:p.Asp1380Gly
NM_001173464.2:c.4250A>G MANE Select	NP_001166935.1:p.Asp1417Gly
NM_001173465.2:c.4091A>G	NP_001166936.1:p.Asp1364Gly
NM_017641.4:c.4211A>G	NP_060111.2:p.Asp1404Gly
NM_001378439.1:c.4253A>G	NP_001365368.1:p.Asp1418Gly
NM_001378440.1:c.4238A>G	NP_001365369.1:p.Asp1413Gly
NM_001378441.1:c.4214A>G	NP_001365370.1:p.Asp1405Gly