Canonical Allele Identifier: CA414844133

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869613C>G (hg19) ; chrY:g.19707727C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707727C>G , CM000686.2:g.19707727C>G	GRCh38
NC_000024.9:g.21869613C>G , CM000686.1:g.21869613C>G	GRCh37
NC_000024.8:g.20329001C>G	NCBI36
NG_032920.1:g.42213G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3419G>C MANE Select	ENSP00000322408.4:p.Gly1140Ala
ENST00000317961.8:c.3419G>C	ENSP00000322408.4:p.Gly1140Ala
ENST00000382806.6:c.3248G>C	ENSP00000372256.2:p.Gly1083Ala
ENST00000415360.1:c.335G>C	ENSP00000389433.1:p.Gly112Ala
ENST00000440077.5:c.3296G>C	ENSP00000398543.1:p.Gly1099Ala
ENST00000469599.6:n.2017G>C
ENST00000492117.1:n.3311G>C
ENST00000541639.5:c.3512G>C	ENSP00000444293.1:p.Gly1171Ala
NM_001146705.1:c.3512G>C	NP_001140177.1:p.Gly1171Ala
NM_001146706.1:c.3248G>C	NP_001140178.1:p.Gly1083Ala
NM_004653.4:c.3419G>C	NP_004644.2:p.Gly1140Ala
XM_005262560.1:c.3284G>C	XP_005262617.1:p.Gly1095Ala
XM_005262561.1:c.3188G>C	XP_005262618.1:p.Gly1063Ala
XM_011531468.1:c.3341G>C	XP_011529770.1:p.Gly1114Ala
XR_244571.2:n.3707G>C
XR_430568.2:n.4041G>C
XM_005262560.3:c.3284G>C	XP_005262617.1:p.Gly1095Ala
XM_005262561.3:c.3188G>C	XP_005262618.1:p.Gly1063Ala
XM_011531468.3:c.3341G>C	XP_011529770.1:p.Gly1114Ala
XM_024452495.1:c.1409G>C	XP_024308263.1:p.Gly470Ala
XM_024452496.1:c.1175G>C	XP_024308264.1:p.Gly392Ala
XR_001756009.2:n.4157G>C
XR_001756010.2:n.4157G>C
XR_001756011.2:n.4022G>C
XR_001756012.2:n.4170G>C
XR_001756013.2:n.3488G>C
XR_002958832.1:n.3589G>C
XR_002958834.1:n.3813G>C
XR_002958835.1:n.3696G>C
XR_002958836.1:n.4379G>C
XR_002958837.1:n.4186G>C
XR_244571.4:n.3706G>C
XR_430568.4:n.4040G>C
NM_001146706.2:c.3248G>C	NP_001140178.1:p.Gly1083Ala
NM_004653.5:c.3419G>C MANE Select	NP_004644.2:p.Gly1140Ala
NM_001146705.2:c.3512G>C	NP_001140177.1:p.Gly1171Ala