Canonical Allele Identifier: CA520160838

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869865C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707979C>T , CM000686.2:g.19707979C>T	GRCh38
NC_000024.9:g.21869865C>T , CM000686.1:g.21869865C>T	GRCh37
NC_000024.8:g.20329253C>T	NCBI36
NG_032920.1:g.41961G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3354G>A MANE Select	ENSP00000322408.4:p.Glu1118=
ENST00000317961.8:c.3354G>A	ENSP00000322408.4:p.Glu1118=
ENST00000382806.6:c.3183G>A	ENSP00000372256.2:p.Glu1061=
ENST00000415360.1:c.270G>A	ENSP00000389433.1:p.Glu90=
ENST00000440077.5:c.3231G>A	ENSP00000398543.1:p.Glu1077=
ENST00000469599.6:n.1952G>A
ENST00000492117.1:n.3246G>A
ENST00000541639.5:c.3447G>A	ENSP00000444293.1:p.Glu1149=
NM_001146705.1:c.3447G>A	NP_001140177.1:p.Glu1149=
NM_001146706.1:c.3183G>A	NP_001140178.1:p.Glu1061=
NM_004653.4:c.3354G>A	NP_004644.2:p.Glu1118=
XM_005262560.1:c.3219G>A	XP_005262617.1:p.Glu1073=
XM_005262561.1:c.3123G>A	XP_005262618.1:p.Glu1041=
XM_011531468.1:c.3276G>A	XP_011529770.1:p.Glu1092=
XR_244571.2:n.3642G>A
XR_430568.2:n.3976G>A
XM_005262560.3:c.3219G>A	XP_005262617.1:p.Glu1073=
XM_005262561.3:c.3123G>A	XP_005262618.1:p.Glu1041=
XM_011531468.3:c.3276G>A	XP_011529770.1:p.Glu1092=
XM_024452495.1:c.1344G>A	XP_024308263.1:p.Glu448=
XM_024452496.1:c.1110G>A	XP_024308264.1:p.Glu370=
XR_001756009.2:n.4092G>A
XR_001756010.2:n.4092G>A
XR_001756011.2:n.3957G>A
XR_001756012.2:n.4105G>A
XR_001756013.2:n.3423G>A
XR_002958832.1:n.3524G>A
XR_002958834.1:n.3748G>A
XR_002958835.1:n.3631G>A
XR_002958836.1:n.4314G>A
XR_002958837.1:n.4121G>A
XR_244571.4:n.3641G>A
XR_430568.4:n.3975G>A
NM_001146706.2:c.3183G>A	NP_001140178.1:p.Glu1061=
NM_004653.5:c.3354G>A MANE Select	NP_004644.2:p.Glu1118=
NM_001146705.2:c.3447G>A	NP_001140177.1:p.Glu1149=