Canonical Allele Identifier: CA414843884

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869529G>A (hg19) ; chrY:g.19707643G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707643G>A , CM000686.2:g.19707643G>A	GRCh38
NC_000024.9:g.21869529G>A , CM000686.1:g.21869529G>A	GRCh37
NC_000024.8:g.20328917G>A	NCBI36
NG_032920.1:g.42297C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3503C>T MANE Select	ENSP00000322408.4:p.Ala1168Val
ENST00000317961.8:c.3503C>T	ENSP00000322408.4:p.Ala1168Val
ENST00000382806.6:c.3332C>T	ENSP00000372256.2:p.Ala1111Val
ENST00000415360.1:c.419C>T	ENSP00000389433.1:p.Ala140Val
ENST00000440077.5:c.3380C>T	ENSP00000398543.1:p.Ala1127Val
ENST00000469599.6:n.2101C>T
ENST00000492117.1:n.3395C>T
ENST00000541639.5:c.3596C>T	ENSP00000444293.1:p.Ala1199Val
NM_001146705.1:c.3596C>T	NP_001140177.1:p.Ala1199Val
NM_001146706.1:c.3332C>T	NP_001140178.1:p.Ala1111Val
NM_004653.4:c.3503C>T	NP_004644.2:p.Ala1168Val
XM_005262560.1:c.3368C>T	XP_005262617.1:p.Ala1123Val
XM_005262561.1:c.3272C>T	XP_005262618.1:p.Ala1091Val
XM_011531468.1:c.3425C>T	XP_011529770.1:p.Ala1142Val
XR_244571.2:n.3791C>T
XR_430568.2:n.4125C>T
XM_005262560.3:c.3368C>T	XP_005262617.1:p.Ala1123Val
XM_005262561.3:c.3272C>T	XP_005262618.1:p.Ala1091Val
XM_011531468.3:c.3425C>T	XP_011529770.1:p.Ala1142Val
XM_024452495.1:c.1493C>T	XP_024308263.1:p.Ala498Val
XM_024452496.1:c.1259C>T	XP_024308264.1:p.Ala420Val
XR_001756009.2:n.4241C>T
XR_001756010.2:n.4241C>T
XR_001756011.2:n.4106C>T
XR_001756012.2:n.4254C>T
XR_001756013.2:n.3572C>T
XR_002958832.1:n.3673C>T
XR_002958834.1:n.3897C>T
XR_002958835.1:n.3780C>T
XR_002958836.1:n.4463C>T
XR_002958837.1:n.4270C>T
XR_244571.4:n.3790C>T
XR_430568.4:n.4124C>T
NM_001146706.2:c.3332C>T	NP_001140178.1:p.Ala1111Val
NM_004653.5:c.3503C>T MANE Select	NP_004644.2:p.Ala1168Val
NM_001146705.2:c.3596C>T	NP_001140177.1:p.Ala1199Val