Canonical Allele Identifier: CA520160840

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869868T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707982T>C , CM000686.2:g.19707982T>C	GRCh38
NC_000024.9:g.21869868T>C , CM000686.1:g.21869868T>C	GRCh37
NC_000024.8:g.20329256T>C	NCBI36
NG_032920.1:g.41958A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.3351A>G MANE Select	ENSP00000322408.4:p.Thr1117=
ENST00000317961.8:c.3351A>G	ENSP00000322408.4:p.Thr1117=
ENST00000382806.6:c.3180A>G	ENSP00000372256.2:p.Thr1060=
ENST00000415360.1:c.267A>G	ENSP00000389433.1:p.Thr89=
ENST00000440077.5:c.3228A>G	ENSP00000398543.1:p.Thr1076=
ENST00000469599.6:n.1949A>G
ENST00000492117.1:n.3243A>G
ENST00000541639.5:c.3444A>G	ENSP00000444293.1:p.Thr1148=
NM_001146705.1:c.3444A>G	NP_001140177.1:p.Thr1148=
NM_001146706.1:c.3180A>G	NP_001140178.1:p.Thr1060=
NM_004653.4:c.3351A>G	NP_004644.2:p.Thr1117=
XM_005262560.1:c.3216A>G	XP_005262617.1:p.Thr1072=
XM_005262561.1:c.3120A>G	XP_005262618.1:p.Thr1040=
XM_011531468.1:c.3273A>G	XP_011529770.1:p.Thr1091=
XR_244571.2:n.3639A>G
XR_430568.2:n.3973A>G
XM_005262560.3:c.3216A>G	XP_005262617.1:p.Thr1072=
XM_005262561.3:c.3120A>G	XP_005262618.1:p.Thr1040=
XM_011531468.3:c.3273A>G	XP_011529770.1:p.Thr1091=
XM_024452495.1:c.1341A>G	XP_024308263.1:p.Thr447=
XM_024452496.1:c.1107A>G	XP_024308264.1:p.Thr369=
XR_001756009.2:n.4089A>G
XR_001756010.2:n.4089A>G
XR_001756011.2:n.3954A>G
XR_001756012.2:n.4102A>G
XR_001756013.2:n.3420A>G
XR_002958832.1:n.3521A>G
XR_002958834.1:n.3745A>G
XR_002958835.1:n.3628A>G
XR_002958836.1:n.4311A>G
XR_002958837.1:n.4118A>G
XR_244571.4:n.3638A>G
XR_430568.4:n.3972A>G
NM_001146706.2:c.3180A>G	NP_001140178.1:p.Thr1060=
NM_004653.5:c.3351A>G MANE Select	NP_004644.2:p.Thr1117=
NM_001146705.2:c.3444A>G	NP_001140177.1:p.Thr1148=