Canonical Allele Identifier: CA414843486

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869422G>T (hg19) ; chrY:g.19707536G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707536G>T , CM000686.2:g.19707536G>T	GRCh38
NC_000024.9:g.21869422G>T , CM000686.1:g.21869422G>T	GRCh37
NC_000024.8:g.20328810G>T	NCBI36
NG_032920.1:g.42404C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3610C>A MANE Select	ENSP00000322408.4:p.Pro1204Thr
ENST00000317961.8:c.3610C>A	ENSP00000322408.4:p.Pro1204Thr
ENST00000382806.6:c.3439C>A	ENSP00000372256.2:p.Pro1147Thr
ENST00000415360.1:c.526C>A	ENSP00000389433.1:p.Pro176Thr
ENST00000440077.5:c.3487C>A	ENSP00000398543.1:p.Pro1163Thr
ENST00000469599.6:n.2208C>A
ENST00000492117.1:n.3502C>A
ENST00000541639.5:c.3703C>A	ENSP00000444293.1:p.Pro1235Thr
NM_001146705.1:c.3703C>A	NP_001140177.1:p.Pro1235Thr
NM_001146706.1:c.3439C>A	NP_001140178.1:p.Pro1147Thr
NM_004653.4:c.3610C>A	NP_004644.2:p.Pro1204Thr
XM_005262560.1:c.3475C>A	XP_005262617.1:p.Pro1159Thr
XM_005262561.1:c.3379C>A	XP_005262618.1:p.Pro1127Thr
XM_011531468.1:c.3532C>A	XP_011529770.1:p.Pro1178Thr
XR_244571.2:n.3898C>A
XR_430568.2:n.4232C>A
XM_005262560.3:c.3475C>A	XP_005262617.1:p.Pro1159Thr
XM_005262561.3:c.3379C>A	XP_005262618.1:p.Pro1127Thr
XM_011531468.3:c.3532C>A	XP_011529770.1:p.Pro1178Thr
XM_024452495.1:c.1600C>A	XP_024308263.1:p.Pro534Thr
XM_024452496.1:c.1366C>A	XP_024308264.1:p.Pro456Thr
XR_001756009.2:n.4348C>A
XR_001756010.2:n.4348C>A
XR_001756011.2:n.4213C>A
XR_001756012.2:n.4361C>A
XR_001756013.2:n.3679C>A
XR_002958832.1:n.3780C>A
XR_002958834.1:n.4004C>A
XR_002958835.1:n.3887C>A
XR_002958836.1:n.4570C>A
XR_002958837.1:n.4377C>A
XR_244571.4:n.3897C>A
XR_430568.4:n.4231C>A
NM_001146706.2:c.3439C>A	NP_001140178.1:p.Pro1147Thr
NM_004653.5:c.3610C>A MANE Select	NP_004644.2:p.Pro1204Thr
NM_001146705.2:c.3703C>A	NP_001140177.1:p.Pro1235Thr