Canonical Allele Identifier: CA414840178

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21867997G>T (hg19) ; chrY:g.19706111G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706111G>T , CM000686.2:g.19706111G>T	GRCh38
NC_000024.9:g.21867997G>T , CM000686.1:g.21867997G>T	GRCh37
NC_000024.8:g.20327385G>T	NCBI36
NG_032920.1:g.43829C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4504C>A MANE Select	ENSP00000322408.4:p.Pro1502Thr
ENST00000317961.8:c.4504C>A	ENSP00000322408.4:p.Pro1502Thr
ENST00000382806.6:c.4333C>A	ENSP00000372256.2:p.Pro1445Thr
ENST00000440077.5:c.4381C>A	ENSP00000398543.1:p.Pro1461Thr
ENST00000469599.6:n.3255C>A
ENST00000492117.1:n.4549C>A
ENST00000541639.5:c.4597C>A	ENSP00000444293.1:p.Pro1533Thr
NM_001146705.1:c.4597C>A	NP_001140177.1:p.Pro1533Thr
NM_001146706.1:c.4333C>A	NP_001140178.1:p.Pro1445Thr
NM_004653.4:c.4504C>A	NP_004644.2:p.Pro1502Thr
XM_005262560.1:c.4369C>A	XP_005262617.1:p.Pro1457Thr
XM_005262561.1:c.4273C>A	XP_005262618.1:p.Pro1425Thr
XM_011531468.1:c.4426C>A	XP_011529770.1:p.Pro1476Thr
XR_430568.2:n.5279C>A
XM_005262560.3:c.4369C>A	XP_005262617.1:p.Pro1457Thr
XM_005262561.3:c.4273C>A	XP_005262618.1:p.Pro1425Thr
XM_011531468.3:c.4426C>A	XP_011529770.1:p.Pro1476Thr
XM_024452495.1:c.2494C>A	XP_024308263.1:p.Pro832Thr
XM_024452496.1:c.2260C>A	XP_024308264.1:p.Pro754Thr
XR_001756009.2:n.5242C>A
XR_001756010.2:n.5210C>A
XR_001756011.2:n.5107C>A
XR_001756012.2:n.5255C>A
XR_001756013.2:n.4573C>A
XR_002958832.1:n.4827C>A
XR_002958834.1:n.4898C>A
XR_002958835.1:n.4781C>A
XR_002958836.1:n.5432C>A
XR_002958837.1:n.5239C>A
XR_244571.4:n.4759C>A
XR_430568.4:n.5278C>A
NM_001146706.2:c.4333C>A	NP_001140178.1:p.Pro1445Thr
NM_004653.5:c.4504C>A MANE Select	NP_004644.2:p.Pro1502Thr
NM_001146705.2:c.4597C>A	NP_001140177.1:p.Pro1533Thr