Canonical Allele Identifier: CA414841419

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21894477A>G (hg19) ; chrY:g.19732591A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19732591A>G , CM000686.2:g.19732591A>G	GRCh38
NC_000024.9:g.21894477A>G , CM000686.1:g.21894477A>G	GRCh37
NC_000024.8:g.20353865A>G	NCBI36
NG_032920.1:g.17349T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.1085T>C MANE Select	ENSP00000322408.4:p.Ile362Thr
ENST00000317961.8:c.1085T>C	ENSP00000322408.4:p.Ile362Thr
ENST00000382806.6:c.914T>C	ENSP00000372256.2:p.Ile305Thr
ENST00000440077.5:c.962T>C	ENSP00000398543.1:p.Ile321Thr
ENST00000447300.1:c.950T>C	ENSP00000416377.1:p.Ile317Thr
ENST00000541639.5:c.1085T>C	ENSP00000444293.1:p.Ile362Thr
NM_001146705.1:c.1085T>C	NP_001140177.1:p.Ile362Thr
NM_001146706.1:c.914T>C	NP_001140178.1:p.Ile305Thr
NM_004653.4:c.1085T>C	NP_004644.2:p.Ile362Thr
XM_005262560.1:c.950T>C	XP_005262617.1:p.Ile317Thr
XM_005262561.1:c.1085T>C	XP_005262618.1:p.Ile362Thr
XM_005262562.2:c.1085T>C	XP_005262619.1:p.Ile362Thr
XM_011531468.1:c.1085T>C	XP_011529770.1:p.Ile362Thr
XR_244571.2:n.1373T>C
XR_430568.2:n.1373T>C
XR_938609.1:n.1373T>C
XR_938610.1:n.1373T>C
XM_005262560.3:c.950T>C	XP_005262617.1:p.Ile317Thr
XM_005262561.3:c.1085T>C	XP_005262618.1:p.Ile362Thr
XM_011531468.3:c.1085T>C	XP_011529770.1:p.Ile362Thr
XM_024452495.1:c.-1033T>C	XP_024308263.1:n.-1033T>C
XR_001756009.2:n.1372T>C
XR_001756010.2:n.1372T>C
XR_001756011.2:n.1237T>C
XR_001756012.2:n.1372T>C
XR_001756013.2:n.1372T>C
XR_002958832.1:n.1372T>C
XR_002958833.1:n.1372T>C
XR_002958834.1:n.1372T>C
XR_002958835.1:n.1372T>C
XR_002958836.1:n.1372T>C
XR_002958837.1:n.1372T>C
XR_244571.4:n.1372T>C
XR_430568.4:n.1372T>C
NM_001146706.2:c.914T>C	NP_001140178.1:p.Ile305Thr
NM_004653.5:c.1085T>C MANE Select	NP_004644.2:p.Ile362Thr
NM_001146705.2:c.1085T>C	NP_001140177.1:p.Ile362Thr