Canonical Allele Identifier: CA520160757

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869570G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707684G>T , CM000686.2:g.19707684G>T	GRCh38
NC_000024.9:g.21869570G>T , CM000686.1:g.21869570G>T	GRCh37
NC_000024.8:g.20328958G>T	NCBI36
NG_032920.1:g.42256C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3462C>A MANE Select	ENSP00000322408.4:p.Thr1154=
ENST00000317961.8:c.3462C>A	ENSP00000322408.4:p.Thr1154=
ENST00000382806.6:c.3291C>A	ENSP00000372256.2:p.Thr1097=
ENST00000415360.1:c.378C>A	ENSP00000389433.1:p.Thr126=
ENST00000440077.5:c.3339C>A	ENSP00000398543.1:p.Thr1113=
ENST00000469599.6:n.2060C>A
ENST00000492117.1:n.3354C>A
ENST00000541639.5:c.3555C>A	ENSP00000444293.1:p.Thr1185=
NM_001146705.1:c.3555C>A	NP_001140177.1:p.Thr1185=
NM_001146706.1:c.3291C>A	NP_001140178.1:p.Thr1097=
NM_004653.4:c.3462C>A	NP_004644.2:p.Thr1154=
XM_005262560.1:c.3327C>A	XP_005262617.1:p.Thr1109=
XM_005262561.1:c.3231C>A	XP_005262618.1:p.Thr1077=
XM_011531468.1:c.3384C>A	XP_011529770.1:p.Thr1128=
XR_244571.2:n.3750C>A
XR_430568.2:n.4084C>A
XM_005262560.3:c.3327C>A	XP_005262617.1:p.Thr1109=
XM_005262561.3:c.3231C>A	XP_005262618.1:p.Thr1077=
XM_011531468.3:c.3384C>A	XP_011529770.1:p.Thr1128=
XM_024452495.1:c.1452C>A	XP_024308263.1:p.Thr484=
XM_024452496.1:c.1218C>A	XP_024308264.1:p.Thr406=
XR_001756009.2:n.4200C>A
XR_001756010.2:n.4200C>A
XR_001756011.2:n.4065C>A
XR_001756012.2:n.4213C>A
XR_001756013.2:n.3531C>A
XR_002958832.1:n.3632C>A
XR_002958834.1:n.3856C>A
XR_002958835.1:n.3739C>A
XR_002958836.1:n.4422C>A
XR_002958837.1:n.4229C>A
XR_244571.4:n.3749C>A
XR_430568.4:n.4083C>A
NM_001146706.2:c.3291C>A	NP_001140178.1:p.Thr1097=
NM_004653.5:c.3462C>A MANE Select	NP_004644.2:p.Thr1154=
NM_001146705.2:c.3555C>A	NP_001140177.1:p.Thr1185=