Canonical Allele Identifier: CA479233356

Gene: KIF21A

Linked Data

• gnomAD v4: 12-39309600-G-A
• MyVariant Identifiers: chr12:g.39703402G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309600G>A , CM000674.2:g.39309600G>A	GRCh38
NC_000012.11:g.39703402G>A , CM000674.1:g.39703402G>A	GRCh37
NC_000012.10:g.37989669G>A	NCBI36
NG_017067.1:g.138791C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4263C>T MANE Select	ENSP00000354878.5:p.Cys1421=
ENST00000636569.1:c.4200C>T	ENSP00000490369.1:p.Cys1400=
ENST00000361418.9:c.4263C>T	ENSP00000354878.5:p.Cys1421=
ENST00000361961.7:c.4224C>T	ENSP00000354851.3:p.Cys1408=
ENST00000541463.6:c.4104C>T	ENSP00000438075.2:p.Cys1368=
ENST00000544797.6:c.4152C>T	ENSP00000445606.2:p.Cys1384=
ENST00000547733.1:n.1577C>T
ENST00000551264.5:c.1206C>T	ENSP00000448792.1:p.Cys402=
ENST00000552961.5:c.2165C>T
NM_001173463.1:c.4152C>T	NP_001166934.1:p.Cys1384=
NM_001173464.1:c.4263C>T	NP_001166935.1:p.Cys1421=
NM_001173465.1:c.4104C>T	NP_001166936.1:p.Cys1368=
NM_017641.3:c.4224C>T	NP_060111.2:p.Cys1408=
XM_005269007.1:c.4266C>T	XP_005269064.1:p.Cys1422=
XM_005269008.1:c.4251C>T	XP_005269065.1:p.Cys1417=
XM_005269009.1:c.4245C>T	XP_005269066.1:p.Cys1415=
XM_005269010.1:c.4227C>T	XP_005269067.1:p.Cys1409=
XM_005269011.1:c.4212C>T	XP_005269068.1:p.Cys1404=
XM_005269012.1:c.4137C>T	XP_005269069.1:p.Cys1379=
XM_005269013.1:c.4122C>T	XP_005269070.1:p.Cys1374=
XM_005269014.1:c.4083C>T	XP_005269071.1:p.Cys1361=
XM_006719493.1:c.4206C>T	XP_006719556.1:p.Cys1402=
XM_006719494.1:c.4134C>T	XP_006719557.1:p.Cys1378=
XM_006719496.1:c.4191C>T	XP_006719559.1:p.Cys1397=
XM_011538556.1:c.4197C>T	XP_011536858.1:p.Cys1399=
XM_005269007.3:c.4266C>T	XP_005269064.1:p.Cys1422=
XM_005269008.3:c.4251C>T	XP_005269065.1:p.Cys1417=
XM_005269009.3:c.4245C>T	XP_005269066.1:p.Cys1415=
XM_005269010.3:c.4227C>T	XP_005269067.1:p.Cys1409=
XM_005269011.3:c.4212C>T	XP_005269068.1:p.Cys1404=
XM_005269012.3:c.4137C>T	XP_005269069.1:p.Cys1379=
XM_005269013.3:c.4122C>T	XP_005269070.1:p.Cys1374=
XM_005269014.3:c.4083C>T	XP_005269071.1:p.Cys1361=
XM_006719493.3:c.4206C>T	XP_006719556.1:p.Cys1402=
XM_006719494.3:c.4134C>T	XP_006719557.1:p.Cys1378=
XM_011538556.3:c.4197C>T	XP_011536858.1:p.Cys1399=
XM_017019607.2:c.4212C>T	XP_016875096.1:p.Cys1404=
XM_017019608.2:c.4173C>T	XP_016875097.1:p.Cys1391=
XM_017019609.2:c.4062C>T	XP_016875098.1:p.Cys1354=
XM_017019610.2:c.4062C>T	XP_016875099.1:p.Cys1354=
XM_017019611.2:c.4044C>T	XP_016875100.1:p.Cys1348=
NM_001173463.2:c.4152C>T	NP_001166934.1:p.Cys1384=
NM_001173464.2:c.4263C>T MANE Select	NP_001166935.1:p.Cys1421=
NM_001173465.2:c.4104C>T	NP_001166936.1:p.Cys1368=
NM_017641.4:c.4224C>T	NP_060111.2:p.Cys1408=
NM_001378439.1:c.4266C>T	NP_001365368.1:p.Cys1422=
NM_001378440.1:c.4251C>T	NP_001365369.1:p.Cys1417=
NM_001378441.1:c.4227C>T	NP_001365370.1:p.Cys1409=