Canonical Allele Identifier: CA414844277

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869833T>G (hg19) ; chrY:g.19707947T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707947T>G , CM000686.2:g.19707947T>G	GRCh38
NC_000024.9:g.21869833T>G , CM000686.1:g.21869833T>G	GRCh37
NC_000024.8:g.20329221T>G	NCBI36
NG_032920.1:g.41993A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3386A>C MANE Select	ENSP00000322408.4:p.Asp1129Ala
ENST00000317961.8:c.3386A>C	ENSP00000322408.4:p.Asp1129Ala
ENST00000382806.6:c.3215A>C	ENSP00000372256.2:p.Asp1072Ala
ENST00000415360.1:c.302A>C	ENSP00000389433.1:p.Asp101Ala
ENST00000440077.5:c.3263A>C	ENSP00000398543.1:p.Asp1088Ala
ENST00000469599.6:n.1984A>C
ENST00000492117.1:n.3278A>C
ENST00000541639.5:c.3479A>C	ENSP00000444293.1:p.Asp1160Ala
NM_001146705.1:c.3479A>C	NP_001140177.1:p.Asp1160Ala
NM_001146706.1:c.3215A>C	NP_001140178.1:p.Asp1072Ala
NM_004653.4:c.3386A>C	NP_004644.2:p.Asp1129Ala
XM_005262560.1:c.3251A>C	XP_005262617.1:p.Asp1084Ala
XM_005262561.1:c.3155A>C	XP_005262618.1:p.Asp1052Ala
XM_011531468.1:c.3308A>C	XP_011529770.1:p.Asp1103Ala
XR_244571.2:n.3674A>C
XR_430568.2:n.4008A>C
XM_005262560.3:c.3251A>C	XP_005262617.1:p.Asp1084Ala
XM_005262561.3:c.3155A>C	XP_005262618.1:p.Asp1052Ala
XM_011531468.3:c.3308A>C	XP_011529770.1:p.Asp1103Ala
XM_024452495.1:c.1376A>C	XP_024308263.1:p.Asp459Ala
XM_024452496.1:c.1142A>C	XP_024308264.1:p.Asp381Ala
XR_001756009.2:n.4124A>C
XR_001756010.2:n.4124A>C
XR_001756011.2:n.3989A>C
XR_001756012.2:n.4137A>C
XR_001756013.2:n.3455A>C
XR_002958832.1:n.3556A>C
XR_002958834.1:n.3780A>C
XR_002958835.1:n.3663A>C
XR_002958836.1:n.4346A>C
XR_002958837.1:n.4153A>C
XR_244571.4:n.3673A>C
XR_430568.4:n.4007A>C
NM_001146706.2:c.3215A>C	NP_001140178.1:p.Asp1072Ala
NM_004653.5:c.3386A>C MANE Select	NP_004644.2:p.Asp1129Ala
NM_001146705.2:c.3479A>C	NP_001140177.1:p.Asp1160Ala