Canonical Allele Identifier: CA2766253164

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707919G>A , CM000686.2:g.19707919G>A	GRCh38
NC_000024.9:g.21869805G>A , CM000686.1:g.21869805G>A	GRCh37
NC_000024.8:g.20329193G>A	NCBI36
NG_032920.1:g.42021C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3399+15C>T MANE Select	ENSP00000322408.4:n.3399+15C>T
ENST00000317961.8:c.3399+15C>T	ENSP00000322408.4:n.3399+15C>T
ENST00000382806.6:c.3228+15C>T	ENSP00000372256.2:n.3228+15C>T
ENST00000415360.1:c.315+15C>T	ENSP00000389433.1:n.315+15C>T
ENST00000440077.5:c.3276+15C>T	ENSP00000398543.1:n.3276+15C>T
ENST00000469599.6:n.1997+15C>T
ENST00000492117.1:n.3291+15C>T
ENST00000541639.5:c.3492+15C>T	ENSP00000444293.1:n.3492+15C>T
NM_001146705.1:c.3492+15C>T	NP_001140177.1:n.3492+15C>T
NM_001146706.1:c.3228+15C>T	NP_001140178.1:n.3228+15C>T
NM_004653.4:c.3399+15C>T	NP_004644.2:n.3399+15C>T
XM_005262560.1:c.3264+15C>T	XP_005262617.1:n.3264+15C>T
XM_005262561.1:c.3168+15C>T	XP_005262618.1:n.3168+15C>T
XM_011531468.1:c.3321+15C>T	XP_011529770.1:n.3321+15C>T
XR_244571.2:n.3687+15C>T
XR_430568.2:n.4021+15C>T
XM_005262560.3:c.3264+15C>T	XP_005262617.1:n.3264+15C>T
XM_005262561.3:c.3168+15C>T	XP_005262618.1:n.3168+15C>T
XM_011531468.3:c.3321+15C>T	XP_011529770.1:n.3321+15C>T
XM_024452495.1:c.1389+15C>T	XP_024308263.1:n.1389+15C>T
XM_024452496.1:c.1155+15C>T	XP_024308264.1:n.1155+15C>T
XR_001756009.2:n.4137+15C>T
XR_001756010.2:n.4137+15C>T
XR_001756011.2:n.4002+15C>T
XR_001756012.2:n.4150+15C>T
XR_001756013.2:n.3468+15C>T
XR_002958832.1:n.3569+15C>T
XR_002958834.1:n.3793+15C>T
XR_002958835.1:n.3676+15C>T
XR_002958836.1:n.4359+15C>T
XR_002958837.1:n.4166+15C>T
XR_244571.4:n.3686+15C>T
XR_430568.4:n.4020+15C>T
NM_001146706.2:c.3228+15C>T	NP_001140178.1:n.3228+15C>T
NM_004653.5:c.3399+15C>T MANE Select	NP_004644.2:n.3399+15C>T
NM_001146705.2:c.3492+15C>T	NP_001140177.1:n.3492+15C>T