Canonical Allele Identifier: CA520516848

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869498C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707612C>G , CM000686.2:g.19707612C>G	GRCh38
NC_000024.9:g.21869498C>G , CM000686.1:g.21869498C>G	GRCh37
NC_000024.8:g.20328886C>G	NCBI36
NG_032920.1:g.42328G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3534G>C MANE Select	ENSP00000322408.4:p.Gly1178=
ENST00000317961.8:c.3534G>C	ENSP00000322408.4:p.Gly1178=
ENST00000382806.6:c.3363G>C	ENSP00000372256.2:p.Gly1121=
ENST00000415360.1:c.450G>C	ENSP00000389433.1:p.Gly150=
ENST00000440077.5:c.3411G>C	ENSP00000398543.1:p.Gly1137=
ENST00000469599.6:n.2132G>C
ENST00000492117.1:n.3426G>C
ENST00000541639.5:c.3627G>C	ENSP00000444293.1:p.Gly1209=
NM_001146705.1:c.3627G>C	NP_001140177.1:p.Gly1209=
NM_001146706.1:c.3363G>C	NP_001140178.1:p.Gly1121=
NM_004653.4:c.3534G>C	NP_004644.2:p.Gly1178=
XM_005262560.1:c.3399G>C	XP_005262617.1:p.Gly1133=
XM_005262561.1:c.3303G>C	XP_005262618.1:p.Gly1101=
XM_011531468.1:c.3456G>C	XP_011529770.1:p.Gly1152=
XR_244571.2:n.3822G>C
XR_430568.2:n.4156G>C
XM_005262560.3:c.3399G>C	XP_005262617.1:p.Gly1133=
XM_005262561.3:c.3303G>C	XP_005262618.1:p.Gly1101=
XM_011531468.3:c.3456G>C	XP_011529770.1:p.Gly1152=
XM_024452495.1:c.1524G>C	XP_024308263.1:p.Gly508=
XM_024452496.1:c.1290G>C	XP_024308264.1:p.Gly430=
XR_001756009.2:n.4272G>C
XR_001756010.2:n.4272G>C
XR_001756011.2:n.4137G>C
XR_001756012.2:n.4285G>C
XR_001756013.2:n.3603G>C
XR_002958832.1:n.3704G>C
XR_002958834.1:n.3928G>C
XR_002958835.1:n.3811G>C
XR_002958836.1:n.4494G>C
XR_002958837.1:n.4301G>C
XR_244571.4:n.3821G>C
XR_430568.4:n.4155G>C
NM_001146706.2:c.3363G>C	NP_001140178.1:p.Gly1121=
NM_004653.5:c.3534G>C MANE Select	NP_004644.2:p.Gly1178=
NM_001146705.2:c.3627G>C	NP_001140177.1:p.Gly1209=