Canonical Allele Identifier: CA414843510

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869430A>G (hg19) ; chrY:g.19707544A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707544A>G , CM000686.2:g.19707544A>G	GRCh38
NC_000024.9:g.21869430A>G , CM000686.1:g.21869430A>G	GRCh37
NC_000024.8:g.20328818A>G	NCBI36
NG_032920.1:g.42396T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3602T>C MANE Select	ENSP00000322408.4:p.Val1201Ala
ENST00000317961.8:c.3602T>C	ENSP00000322408.4:p.Val1201Ala
ENST00000382806.6:c.3431T>C	ENSP00000372256.2:p.Val1144Ala
ENST00000415360.1:c.518T>C	ENSP00000389433.1:p.Val173Ala
ENST00000440077.5:c.3479T>C	ENSP00000398543.1:p.Val1160Ala
ENST00000469599.6:n.2200T>C
ENST00000492117.1:n.3494T>C
ENST00000541639.5:c.3695T>C	ENSP00000444293.1:p.Val1232Ala
NM_001146705.1:c.3695T>C	NP_001140177.1:p.Val1232Ala
NM_001146706.1:c.3431T>C	NP_001140178.1:p.Val1144Ala
NM_004653.4:c.3602T>C	NP_004644.2:p.Val1201Ala
XM_005262560.1:c.3467T>C	XP_005262617.1:p.Val1156Ala
XM_005262561.1:c.3371T>C	XP_005262618.1:p.Val1124Ala
XM_011531468.1:c.3524T>C	XP_011529770.1:p.Val1175Ala
XR_244571.2:n.3890T>C
XR_430568.2:n.4224T>C
XM_005262560.3:c.3467T>C	XP_005262617.1:p.Val1156Ala
XM_005262561.3:c.3371T>C	XP_005262618.1:p.Val1124Ala
XM_011531468.3:c.3524T>C	XP_011529770.1:p.Val1175Ala
XM_024452495.1:c.1592T>C	XP_024308263.1:p.Val531Ala
XM_024452496.1:c.1358T>C	XP_024308264.1:p.Val453Ala
XR_001756009.2:n.4340T>C
XR_001756010.2:n.4340T>C
XR_001756011.2:n.4205T>C
XR_001756012.2:n.4353T>C
XR_001756013.2:n.3671T>C
XR_002958832.1:n.3772T>C
XR_002958834.1:n.3996T>C
XR_002958835.1:n.3879T>C
XR_002958836.1:n.4562T>C
XR_002958837.1:n.4369T>C
XR_244571.4:n.3889T>C
XR_430568.4:n.4223T>C
NM_001146706.2:c.3431T>C	NP_001140178.1:p.Val1144Ala
NM_004653.5:c.3602T>C MANE Select	NP_004644.2:p.Val1201Ala
NM_001146705.2:c.3695T>C	NP_001140177.1:p.Val1232Ala