Canonical Allele Identifier: CA414844759

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869948G>T (hg19) ; chrY:g.19708062G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708062G>T , CM000686.2:g.19708062G>T	GRCh38
NC_000024.9:g.21869948G>T , CM000686.1:g.21869948G>T	GRCh37
NC_000024.8:g.20329336G>T	NCBI36
NG_032920.1:g.41878C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3271C>A MANE Select	ENSP00000322408.4:p.Pro1091Thr
ENST00000317961.8:c.3271C>A	ENSP00000322408.4:p.Pro1091Thr
ENST00000382806.6:c.3100C>A	ENSP00000372256.2:p.Pro1034Thr
ENST00000415360.1:c.187C>A	ENSP00000389433.1:p.Pro63Thr
ENST00000440077.5:c.3148C>A	ENSP00000398543.1:p.Pro1050Thr
ENST00000469599.6:n.1869C>A
ENST00000492117.1:n.3163C>A
ENST00000541639.5:c.3364C>A	ENSP00000444293.1:p.Pro1122Thr
NM_001146705.1:c.3364C>A	NP_001140177.1:p.Pro1122Thr
NM_001146706.1:c.3100C>A	NP_001140178.1:p.Pro1034Thr
NM_004653.4:c.3271C>A	NP_004644.2:p.Pro1091Thr
XM_005262560.1:c.3136C>A	XP_005262617.1:p.Pro1046Thr
XM_005262561.1:c.3040C>A	XP_005262618.1:p.Pro1014Thr
XM_011531468.1:c.3193C>A	XP_011529770.1:p.Pro1065Thr
XR_244571.2:n.3559C>A
XR_430568.2:n.3893C>A
XM_005262560.3:c.3136C>A	XP_005262617.1:p.Pro1046Thr
XM_005262561.3:c.3040C>A	XP_005262618.1:p.Pro1014Thr
XM_011531468.3:c.3193C>A	XP_011529770.1:p.Pro1065Thr
XM_024452495.1:c.1261C>A	XP_024308263.1:p.Pro421Thr
XM_024452496.1:c.1027C>A	XP_024308264.1:p.Pro343Thr
XR_001756009.2:n.4009C>A
XR_001756010.2:n.4009C>A
XR_001756011.2:n.3874C>A
XR_001756012.2:n.4022C>A
XR_001756013.2:n.3340C>A
XR_002958832.1:n.3441C>A
XR_002958834.1:n.3665C>A
XR_002958835.1:n.3548C>A
XR_002958836.1:n.4231C>A
XR_002958837.1:n.4038C>A
XR_244571.4:n.3558C>A
XR_430568.4:n.3892C>A
NM_001146706.2:c.3100C>A	NP_001140178.1:p.Pro1034Thr
NM_004653.5:c.3271C>A MANE Select	NP_004644.2:p.Pro1091Thr
NM_001146705.2:c.3364C>A	NP_001140177.1:p.Pro1122Thr