Canonical Allele Identifier: CA520160830

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869859C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707973C>A , CM000686.2:g.19707973C>A	GRCh38
NC_000024.9:g.21869859C>A , CM000686.1:g.21869859C>A	GRCh37
NC_000024.8:g.20329247C>A	NCBI36
NG_032920.1:g.41967G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.3360G>T MANE Select	ENSP00000322408.4:p.Leu1120=
ENST00000317961.8:c.3360G>T	ENSP00000322408.4:p.Leu1120=
ENST00000382806.6:c.3189G>T	ENSP00000372256.2:p.Leu1063=
ENST00000415360.1:c.276G>T	ENSP00000389433.1:p.Leu92=
ENST00000440077.5:c.3237G>T	ENSP00000398543.1:p.Leu1079=
ENST00000469599.6:n.1958G>T
ENST00000492117.1:n.3252G>T
ENST00000541639.5:c.3453G>T	ENSP00000444293.1:p.Leu1151=
NM_001146705.1:c.3453G>T	NP_001140177.1:p.Leu1151=
NM_001146706.1:c.3189G>T	NP_001140178.1:p.Leu1063=
NM_004653.4:c.3360G>T	NP_004644.2:p.Leu1120=
XM_005262560.1:c.3225G>T	XP_005262617.1:p.Leu1075=
XM_005262561.1:c.3129G>T	XP_005262618.1:p.Leu1043=
XM_011531468.1:c.3282G>T	XP_011529770.1:p.Leu1094=
XR_244571.2:n.3648G>T
XR_430568.2:n.3982G>T
XM_005262560.3:c.3225G>T	XP_005262617.1:p.Leu1075=
XM_005262561.3:c.3129G>T	XP_005262618.1:p.Leu1043=
XM_011531468.3:c.3282G>T	XP_011529770.1:p.Leu1094=
XM_024452495.1:c.1350G>T	XP_024308263.1:p.Leu450=
XM_024452496.1:c.1116G>T	XP_024308264.1:p.Leu372=
XR_001756009.2:n.4098G>T
XR_001756010.2:n.4098G>T
XR_001756011.2:n.3963G>T
XR_001756012.2:n.4111G>T
XR_001756013.2:n.3429G>T
XR_002958832.1:n.3530G>T
XR_002958834.1:n.3754G>T
XR_002958835.1:n.3637G>T
XR_002958836.1:n.4320G>T
XR_002958837.1:n.4127G>T
XR_244571.4:n.3647G>T
XR_430568.4:n.3981G>T
NM_001146706.2:c.3189G>T	NP_001140178.1:p.Leu1063=
NM_004653.5:c.3360G>T MANE Select	NP_004644.2:p.Leu1120=
NM_001146705.2:c.3453G>T	NP_001140177.1:p.Leu1151=