Canonical Allele Identifier: CA414844026

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869568T>G (hg19) ; chrY:g.19707682T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707682T>G , CM000686.2:g.19707682T>G	GRCh38
NC_000024.9:g.21869568T>G , CM000686.1:g.21869568T>G	GRCh37
NC_000024.8:g.20328956T>G	NCBI36
NG_032920.1:g.42258A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3464A>C MANE Select	ENSP00000322408.4:p.Asn1155Thr
ENST00000317961.8:c.3464A>C	ENSP00000322408.4:p.Asn1155Thr
ENST00000382806.6:c.3293A>C	ENSP00000372256.2:p.Asn1098Thr
ENST00000415360.1:c.380A>C	ENSP00000389433.1:p.Asn127Thr
ENST00000440077.5:c.3341A>C	ENSP00000398543.1:p.Asn1114Thr
ENST00000469599.6:n.2062A>C
ENST00000492117.1:n.3356A>C
ENST00000541639.5:c.3557A>C	ENSP00000444293.1:p.Asn1186Thr
NM_001146705.1:c.3557A>C	NP_001140177.1:p.Asn1186Thr
NM_001146706.1:c.3293A>C	NP_001140178.1:p.Asn1098Thr
NM_004653.4:c.3464A>C	NP_004644.2:p.Asn1155Thr
XM_005262560.1:c.3329A>C	XP_005262617.1:p.Asn1110Thr
XM_005262561.1:c.3233A>C	XP_005262618.1:p.Asn1078Thr
XM_011531468.1:c.3386A>C	XP_011529770.1:p.Asn1129Thr
XR_244571.2:n.3752A>C
XR_430568.2:n.4086A>C
XM_005262560.3:c.3329A>C	XP_005262617.1:p.Asn1110Thr
XM_005262561.3:c.3233A>C	XP_005262618.1:p.Asn1078Thr
XM_011531468.3:c.3386A>C	XP_011529770.1:p.Asn1129Thr
XM_024452495.1:c.1454A>C	XP_024308263.1:p.Asn485Thr
XM_024452496.1:c.1220A>C	XP_024308264.1:p.Asn407Thr
XR_001756009.2:n.4202A>C
XR_001756010.2:n.4202A>C
XR_001756011.2:n.4067A>C
XR_001756012.2:n.4215A>C
XR_001756013.2:n.3533A>C
XR_002958832.1:n.3634A>C
XR_002958834.1:n.3858A>C
XR_002958835.1:n.3741A>C
XR_002958836.1:n.4424A>C
XR_002958837.1:n.4231A>C
XR_244571.4:n.3751A>C
XR_430568.4:n.4085A>C
NM_001146706.2:c.3293A>C	NP_001140178.1:p.Asn1098Thr
NM_004653.5:c.3464A>C MANE Select	NP_004644.2:p.Asn1155Thr
NM_001146705.2:c.3557A>C	NP_001140177.1:p.Asn1186Thr