Canonical Allele Identifier: CA2470920689

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19732747_19732750delinsCAAA , CM000686.2:g.19732747_19732750delinsCAAA	GRCh38
NC_000024.9:g.21894633_21894636delinsCAAA , CM000686.1:g.21894633_21894636delinsCAAA	GRCh37
NC_000024.8:g.20354021_20354024delinsCAAA	NCBI36
NG_032920.1:g.17190_17193delinsTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.934-8_934-5delinsTTTG MANE Select	ENSP00000322408.4:n.934-8_934-5delinsTTTG
ENST00000317961.8:c.934-8_934-5delinsTTTG	ENSP00000322408.4:n.934-8_934-5delinsTTTG
ENST00000382806.6:c.763-8_763-5delinsTTTG	ENSP00000372256.2:n.763-8_763-5delinsTTTG
ENST00000440077.5:c.811-8_811-5delinsTTTG	ENSP00000398543.1:n.811-8_811-5delinsTTTG
ENST00000447300.1:c.799-8_799-5delinsTTTG	ENSP00000416377.1:n.799-8_799-5delinsTTTG
ENST00000541639.5:c.934-8_934-5delinsTTTG	ENSP00000444293.1:n.934-8_934-5delinsTTTG
NM_001146705.1:c.934-8_934-5delinsTTTG	NP_001140177.1:n.934-8_934-5delinsTTTG
NM_001146706.1:c.763-8_763-5delinsTTTG	NP_001140178.1:n.763-8_763-5delinsTTTG
NM_004653.4:c.934-8_934-5delinsTTTG	NP_004644.2:n.934-8_934-5delinsTTTG
XM_005262560.1:c.799-8_799-5delinsTTTG	XP_005262617.1:n.799-8_799-5delinsTTTG
XM_005262561.1:c.934-8_934-5delinsTTTG	XP_005262618.1:n.934-8_934-5delinsTTTG
XM_005262562.2:c.934-8_934-5delinsTTTG	XP_005262619.1:n.934-8_934-5delinsTTTG
XM_011531468.1:c.934-8_934-5delinsTTTG	XP_011529770.1:n.934-8_934-5delinsTTTG
XR_244571.2:n.1222-8_1222-5delinsTTTG
XR_430568.2:n.1222-8_1222-5delinsTTTG
XR_938609.1:n.1222-8_1222-5delinsTTTG
XR_938610.1:n.1222-8_1222-5delinsTTTG
XM_005262560.3:c.799-8_799-5delinsTTTG	XP_005262617.1:n.799-8_799-5delinsTTTG
XM_005262561.3:c.934-8_934-5delinsTTTG	XP_005262618.1:n.934-8_934-5delinsTTTG
XM_011531468.3:c.934-8_934-5delinsTTTG	XP_011529770.1:n.934-8_934-5delinsTTTG
XM_024452495.1:c.-1184-8_-1184-5delinsTTTG	XP_024308263.1:n.-1184-8_-1184-5delinsTTTG
XR_001756009.2:n.1221-8_1221-5delinsTTTG
XR_001756010.2:n.1221-8_1221-5delinsTTTG
XR_001756011.2:n.1086-8_1086-5delinsTTTG
XR_001756012.2:n.1221-8_1221-5delinsTTTG
XR_001756013.2:n.1221-8_1221-5delinsTTTG
XR_002958832.1:n.1221-8_1221-5delinsTTTG
XR_002958833.1:n.1221-8_1221-5delinsTTTG
XR_002958834.1:n.1221-8_1221-5delinsTTTG
XR_002958835.1:n.1221-8_1221-5delinsTTTG
XR_002958836.1:n.1221-8_1221-5delinsTTTG
XR_002958837.1:n.1221-8_1221-5delinsTTTG
XR_244571.4:n.1221-8_1221-5delinsTTTG
XR_430568.4:n.1221-8_1221-5delinsTTTG
NM_001146706.2:c.763-8_763-5delinsTTTG	NP_001140178.1:n.763-8_763-5delinsTTTG
NM_004653.5:c.934-8_934-5delinsTTTG MANE Select	NP_004644.2:n.934-8_934-5delinsTTTG
NM_001146705.2:c.934-8_934-5delinsTTTG	NP_001140177.1:n.934-8_934-5delinsTTTG