Canonical Allele Identifier: CA414841890

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868691C>G (hg19) ; chrY:g.19706805C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706805C>G , CM000686.2:g.19706805C>G	GRCh38
NC_000024.9:g.21868691C>G , CM000686.1:g.21868691C>G	GRCh37
NC_000024.8:g.20328079C>G	NCBI36
NG_032920.1:g.43135G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4058G>C MANE Select	ENSP00000322408.4:p.Gly1353Ala
ENST00000317961.8:c.4058G>C	ENSP00000322408.4:p.Gly1353Ala
ENST00000382806.6:c.3887G>C	ENSP00000372256.2:p.Gly1296Ala
ENST00000440077.5:c.3935G>C	ENSP00000398543.1:p.Gly1312Ala
ENST00000469599.6:n.2656G>C
ENST00000492117.1:n.3950G>C
ENST00000541639.5:c.4151G>C	ENSP00000444293.1:p.Gly1384Ala
NM_001146705.1:c.4151G>C	NP_001140177.1:p.Gly1384Ala
NM_001146706.1:c.3887G>C	NP_001140178.1:p.Gly1296Ala
NM_004653.4:c.4058G>C	NP_004644.2:p.Gly1353Ala
XM_005262560.1:c.3923G>C	XP_005262617.1:p.Gly1308Ala
XM_005262561.1:c.3827G>C	XP_005262618.1:p.Gly1276Ala
XM_011531468.1:c.3980G>C	XP_011529770.1:p.Gly1327Ala
XR_244571.2:n.4346G>C
XR_430568.2:n.4680G>C
XM_005262560.3:c.3923G>C	XP_005262617.1:p.Gly1308Ala
XM_005262561.3:c.3827G>C	XP_005262618.1:p.Gly1276Ala
XM_011531468.3:c.3980G>C	XP_011529770.1:p.Gly1327Ala
XM_024452495.1:c.2048G>C	XP_024308263.1:p.Gly683Ala
XM_024452496.1:c.1814G>C	XP_024308264.1:p.Gly605Ala
XR_001756009.2:n.4796G>C
XR_001756010.2:n.4796G>C
XR_001756011.2:n.4661G>C
XR_001756012.2:n.4809G>C
XR_001756013.2:n.4127G>C
XR_002958832.1:n.4228G>C
XR_002958834.1:n.4452G>C
XR_002958835.1:n.4335G>C
XR_002958836.1:n.5018G>C
XR_002958837.1:n.4825G>C
XR_244571.4:n.4345G>C
XR_430568.4:n.4679G>C
NM_001146706.2:c.3887G>C	NP_001140178.1:p.Gly1296Ala
NM_004653.5:c.4058G>C MANE Select	NP_004644.2:p.Gly1353Ala
NM_001146705.2:c.4151G>C	NP_001140177.1:p.Gly1384Ala