Canonical Allele Identifier: CA520160858

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869907C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708021C>A , CM000686.2:g.19708021C>A	GRCh38
NC_000024.9:g.21869907C>A , CM000686.1:g.21869907C>A	GRCh37
NC_000024.8:g.20329295C>A	NCBI36
NG_032920.1:g.41919G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3312G>T MANE Select	ENSP00000322408.4:p.Arg1104=
ENST00000317961.8:c.3312G>T	ENSP00000322408.4:p.Arg1104=
ENST00000382806.6:c.3141G>T	ENSP00000372256.2:p.Arg1047=
ENST00000415360.1:c.228G>T	ENSP00000389433.1:p.Arg76=
ENST00000440077.5:c.3189G>T	ENSP00000398543.1:p.Arg1063=
ENST00000469599.6:n.1910G>T
ENST00000492117.1:n.3204G>T
ENST00000541639.5:c.3405G>T	ENSP00000444293.1:p.Arg1135=
NM_001146705.1:c.3405G>T	NP_001140177.1:p.Arg1135=
NM_001146706.1:c.3141G>T	NP_001140178.1:p.Arg1047=
NM_004653.4:c.3312G>T	NP_004644.2:p.Arg1104=
XM_005262560.1:c.3177G>T	XP_005262617.1:p.Arg1059=
XM_005262561.1:c.3081G>T	XP_005262618.1:p.Arg1027=
XM_011531468.1:c.3234G>T	XP_011529770.1:p.Arg1078=
XR_244571.2:n.3600G>T
XR_430568.2:n.3934G>T
XM_005262560.3:c.3177G>T	XP_005262617.1:p.Arg1059=
XM_005262561.3:c.3081G>T	XP_005262618.1:p.Arg1027=
XM_011531468.3:c.3234G>T	XP_011529770.1:p.Arg1078=
XM_024452495.1:c.1302G>T	XP_024308263.1:p.Arg434=
XM_024452496.1:c.1068G>T	XP_024308264.1:p.Arg356=
XR_001756009.2:n.4050G>T
XR_001756010.2:n.4050G>T
XR_001756011.2:n.3915G>T
XR_001756012.2:n.4063G>T
XR_001756013.2:n.3381G>T
XR_002958832.1:n.3482G>T
XR_002958834.1:n.3706G>T
XR_002958835.1:n.3589G>T
XR_002958836.1:n.4272G>T
XR_002958837.1:n.4079G>T
XR_244571.4:n.3599G>T
XR_430568.4:n.3933G>T
NM_001146706.2:c.3141G>T	NP_001140178.1:p.Arg1047=
NM_004653.5:c.3312G>T MANE Select	NP_004644.2:p.Arg1104=
NM_001146705.2:c.3405G>T	NP_001140177.1:p.Arg1135=