Canonical Allele Identifier: CA520514814

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868052A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706166A>G , CM000686.2:g.19706166A>G	GRCh38
NC_000024.9:g.21868052A>G , CM000686.1:g.21868052A>G	GRCh37
NC_000024.8:g.20327440A>G	NCBI36
NG_032920.1:g.43774T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4449T>C MANE Select	ENSP00000322408.4:p.Tyr1483=
ENST00000317961.8:c.4449T>C	ENSP00000322408.4:p.Tyr1483=
ENST00000382806.6:c.4278T>C	ENSP00000372256.2:p.Tyr1426=
ENST00000440077.5:c.4326T>C	ENSP00000398543.1:p.Tyr1442=
ENST00000469599.6:n.3200T>C
ENST00000492117.1:n.4494T>C
ENST00000541639.5:c.4542T>C	ENSP00000444293.1:p.Tyr1514=
NM_001146705.1:c.4542T>C	NP_001140177.1:p.Tyr1514=
NM_001146706.1:c.4278T>C	NP_001140178.1:p.Tyr1426=
NM_004653.4:c.4449T>C	NP_004644.2:p.Tyr1483=
XM_005262560.1:c.4314T>C	XP_005262617.1:p.Tyr1438=
XM_005262561.1:c.4218T>C	XP_005262618.1:p.Tyr1406=
XM_011531468.1:c.4371T>C	XP_011529770.1:p.Tyr1457=
XR_430568.2:n.5224T>C
XM_005262560.3:c.4314T>C	XP_005262617.1:p.Tyr1438=
XM_005262561.3:c.4218T>C	XP_005262618.1:p.Tyr1406=
XM_011531468.3:c.4371T>C	XP_011529770.1:p.Tyr1457=
XM_024452495.1:c.2439T>C	XP_024308263.1:p.Tyr813=
XM_024452496.1:c.2205T>C	XP_024308264.1:p.Tyr735=
XR_001756009.2:n.5187T>C
XR_001756010.2:n.5155T>C
XR_001756011.2:n.5052T>C
XR_001756012.2:n.5200T>C
XR_001756013.2:n.4518T>C
XR_002958832.1:n.4772T>C
XR_002958834.1:n.4843T>C
XR_002958835.1:n.4726T>C
XR_002958836.1:n.5377T>C
XR_002958837.1:n.5184T>C
XR_244571.4:n.4704T>C
XR_430568.4:n.5223T>C
NM_001146706.2:c.4278T>C	NP_001140178.1:p.Tyr1426=
NM_004653.5:c.4449T>C MANE Select	NP_004644.2:p.Tyr1483=
NM_001146705.2:c.4542T>C	NP_001140177.1:p.Tyr1514=