Canonical Allele Identifier: CA414843303

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869368A>C (hg19) ; chrY:g.19707482A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707482A>C , CM000686.2:g.19707482A>C	GRCh38
NC_000024.9:g.21869368A>C , CM000686.1:g.21869368A>C	GRCh37
NC_000024.8:g.20328756A>C	NCBI36
NG_032920.1:g.42458T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3664T>G MANE Select	ENSP00000322408.4:p.Trp1222Gly
ENST00000317961.8:c.3664T>G	ENSP00000322408.4:p.Trp1222Gly
ENST00000382806.6:c.3493T>G	ENSP00000372256.2:p.Trp1165Gly
ENST00000415360.1:c.580T>G	ENSP00000389433.1:p.Trp194Gly
ENST00000440077.5:c.3541T>G	ENSP00000398543.1:p.Trp1181Gly
ENST00000469599.6:n.2262T>G
ENST00000492117.1:n.3556T>G
ENST00000541639.5:c.3757T>G	ENSP00000444293.1:p.Trp1253Gly
NM_001146705.1:c.3757T>G	NP_001140177.1:p.Trp1253Gly
NM_001146706.1:c.3493T>G	NP_001140178.1:p.Trp1165Gly
NM_004653.4:c.3664T>G	NP_004644.2:p.Trp1222Gly
XM_005262560.1:c.3529T>G	XP_005262617.1:p.Trp1177Gly
XM_005262561.1:c.3433T>G	XP_005262618.1:p.Trp1145Gly
XM_011531468.1:c.3586T>G	XP_011529770.1:p.Trp1196Gly
XR_244571.2:n.3952T>G
XR_430568.2:n.4286T>G
XM_005262560.3:c.3529T>G	XP_005262617.1:p.Trp1177Gly
XM_005262561.3:c.3433T>G	XP_005262618.1:p.Trp1145Gly
XM_011531468.3:c.3586T>G	XP_011529770.1:p.Trp1196Gly
XM_024452495.1:c.1654T>G	XP_024308263.1:p.Trp552Gly
XM_024452496.1:c.1420T>G	XP_024308264.1:p.Trp474Gly
XR_001756009.2:n.4402T>G
XR_001756010.2:n.4402T>G
XR_001756011.2:n.4267T>G
XR_001756012.2:n.4415T>G
XR_001756013.2:n.3733T>G
XR_002958832.1:n.3834T>G
XR_002958834.1:n.4058T>G
XR_002958835.1:n.3941T>G
XR_002958836.1:n.4624T>G
XR_002958837.1:n.4431T>G
XR_244571.4:n.3951T>G
XR_430568.4:n.4285T>G
NM_001146706.2:c.3493T>G	NP_001140178.1:p.Trp1165Gly
NM_004653.5:c.3664T>G MANE Select	NP_004644.2:p.Trp1222Gly
NM_001146705.2:c.3757T>G	NP_001140177.1:p.Trp1253Gly