Canonical Allele Identifier: CA520160754

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869567G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707681G>A , CM000686.2:g.19707681G>A	GRCh38
NC_000024.9:g.21869567G>A , CM000686.1:g.21869567G>A	GRCh37
NC_000024.8:g.20328955G>A	NCBI36
NG_032920.1:g.42259C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3465C>T MANE Select	ENSP00000322408.4:p.Asn1155=
ENST00000317961.8:c.3465C>T	ENSP00000322408.4:p.Asn1155=
ENST00000382806.6:c.3294C>T	ENSP00000372256.2:p.Asn1098=
ENST00000415360.1:c.381C>T	ENSP00000389433.1:p.Asn127=
ENST00000440077.5:c.3342C>T	ENSP00000398543.1:p.Asn1114=
ENST00000469599.6:n.2063C>T
ENST00000492117.1:n.3357C>T
ENST00000541639.5:c.3558C>T	ENSP00000444293.1:p.Asn1186=
NM_001146705.1:c.3558C>T	NP_001140177.1:p.Asn1186=
NM_001146706.1:c.3294C>T	NP_001140178.1:p.Asn1098=
NM_004653.4:c.3465C>T	NP_004644.2:p.Asn1155=
XM_005262560.1:c.3330C>T	XP_005262617.1:p.Asn1110=
XM_005262561.1:c.3234C>T	XP_005262618.1:p.Asn1078=
XM_011531468.1:c.3387C>T	XP_011529770.1:p.Asn1129=
XR_244571.2:n.3753C>T
XR_430568.2:n.4087C>T
XM_005262560.3:c.3330C>T	XP_005262617.1:p.Asn1110=
XM_005262561.3:c.3234C>T	XP_005262618.1:p.Asn1078=
XM_011531468.3:c.3387C>T	XP_011529770.1:p.Asn1129=
XM_024452495.1:c.1455C>T	XP_024308263.1:p.Asn485=
XM_024452496.1:c.1221C>T	XP_024308264.1:p.Asn407=
XR_001756009.2:n.4203C>T
XR_001756010.2:n.4203C>T
XR_001756011.2:n.4068C>T
XR_001756012.2:n.4216C>T
XR_001756013.2:n.3534C>T
XR_002958832.1:n.3635C>T
XR_002958834.1:n.3859C>T
XR_002958835.1:n.3742C>T
XR_002958836.1:n.4425C>T
XR_002958837.1:n.4232C>T
XR_244571.4:n.3752C>T
XR_430568.4:n.4086C>T
NM_001146706.2:c.3294C>T	NP_001140178.1:p.Asn1098=
NM_004653.5:c.3465C>T MANE Select	NP_004644.2:p.Asn1155=
NM_001146705.2:c.3558C>T	NP_001140177.1:p.Asn1186=