Canonical Allele Identifier: CA414843120

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869317G>C (hg19) ; chrY:g.19707431G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707431G>C , CM000686.2:g.19707431G>C	GRCh38
NC_000024.9:g.21869317G>C , CM000686.1:g.21869317G>C	GRCh37
NC_000024.8:g.20328705G>C	NCBI36
NG_032920.1:g.42509C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3715C>G MANE Select	ENSP00000322408.4:p.Arg1239Gly
ENST00000317961.8:c.3715C>G	ENSP00000322408.4:p.Arg1239Gly
ENST00000382806.6:c.3544C>G	ENSP00000372256.2:p.Arg1182Gly
ENST00000415360.1:c.631C>G	ENSP00000389433.1:p.Arg211Gly
ENST00000440077.5:c.3592C>G	ENSP00000398543.1:p.Arg1198Gly
ENST00000469599.6:n.2313C>G
ENST00000492117.1:n.3607C>G
ENST00000541639.5:c.3808C>G	ENSP00000444293.1:p.Arg1270Gly
NM_001146705.1:c.3808C>G	NP_001140177.1:p.Arg1270Gly
NM_001146706.1:c.3544C>G	NP_001140178.1:p.Arg1182Gly
NM_004653.4:c.3715C>G	NP_004644.2:p.Arg1239Gly
XM_005262560.1:c.3580C>G	XP_005262617.1:p.Arg1194Gly
XM_005262561.1:c.3484C>G	XP_005262618.1:p.Arg1162Gly
XM_011531468.1:c.3637C>G	XP_011529770.1:p.Arg1213Gly
XR_244571.2:n.4003C>G
XR_430568.2:n.4337C>G
XM_005262560.3:c.3580C>G	XP_005262617.1:p.Arg1194Gly
XM_005262561.3:c.3484C>G	XP_005262618.1:p.Arg1162Gly
XM_011531468.3:c.3637C>G	XP_011529770.1:p.Arg1213Gly
XM_024452495.1:c.1705C>G	XP_024308263.1:p.Arg569Gly
XM_024452496.1:c.1471C>G	XP_024308264.1:p.Arg491Gly
XR_001756009.2:n.4453C>G
XR_001756010.2:n.4453C>G
XR_001756011.2:n.4318C>G
XR_001756012.2:n.4466C>G
XR_001756013.2:n.3784C>G
XR_002958832.1:n.3885C>G
XR_002958834.1:n.4109C>G
XR_002958835.1:n.3992C>G
XR_002958836.1:n.4675C>G
XR_002958837.1:n.4482C>G
XR_244571.4:n.4002C>G
XR_430568.4:n.4336C>G
NM_001146706.2:c.3544C>G	NP_001140178.1:p.Arg1182Gly
NM_004653.5:c.3715C>G MANE Select	NP_004644.2:p.Arg1239Gly
NM_001146705.2:c.3808C>G	NP_001140177.1:p.Arg1270Gly