Canonical Allele Identifier: CA414844266

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869830G>T (hg19) ; chrY:g.19707944G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707944G>T , CM000686.2:g.19707944G>T	GRCh38
NC_000024.9:g.21869830G>T , CM000686.1:g.21869830G>T	GRCh37
NC_000024.8:g.20329218G>T	NCBI36
NG_032920.1:g.41996C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.3389C>A MANE Select	ENSP00000322408.4:p.Pro1130Gln
ENST00000317961.8:c.3389C>A	ENSP00000322408.4:p.Pro1130Gln
ENST00000382806.6:c.3218C>A	ENSP00000372256.2:p.Pro1073Gln
ENST00000415360.1:c.305C>A	ENSP00000389433.1:p.Pro102Gln
ENST00000440077.5:c.3266C>A	ENSP00000398543.1:p.Pro1089Gln
ENST00000469599.6:n.1987C>A
ENST00000492117.1:n.3281C>A
ENST00000541639.5:c.3482C>A	ENSP00000444293.1:p.Pro1161Gln
NM_001146705.1:c.3482C>A	NP_001140177.1:p.Pro1161Gln
NM_001146706.1:c.3218C>A	NP_001140178.1:p.Pro1073Gln
NM_004653.4:c.3389C>A	NP_004644.2:p.Pro1130Gln
XM_005262560.1:c.3254C>A	XP_005262617.1:p.Pro1085Gln
XM_005262561.1:c.3158C>A	XP_005262618.1:p.Pro1053Gln
XM_011531468.1:c.3311C>A	XP_011529770.1:p.Pro1104Gln
XR_244571.2:n.3677C>A
XR_430568.2:n.4011C>A
XM_005262560.3:c.3254C>A	XP_005262617.1:p.Pro1085Gln
XM_005262561.3:c.3158C>A	XP_005262618.1:p.Pro1053Gln
XM_011531468.3:c.3311C>A	XP_011529770.1:p.Pro1104Gln
XM_024452495.1:c.1379C>A	XP_024308263.1:p.Pro460Gln
XM_024452496.1:c.1145C>A	XP_024308264.1:p.Pro382Gln
XR_001756009.2:n.4127C>A
XR_001756010.2:n.4127C>A
XR_001756011.2:n.3992C>A
XR_001756012.2:n.4140C>A
XR_001756013.2:n.3458C>A
XR_002958832.1:n.3559C>A
XR_002958834.1:n.3783C>A
XR_002958835.1:n.3666C>A
XR_002958836.1:n.4349C>A
XR_002958837.1:n.4156C>A
XR_244571.4:n.3676C>A
XR_430568.4:n.4010C>A
NM_001146706.2:c.3218C>A	NP_001140178.1:p.Pro1073Gln
NM_004653.5:c.3389C>A MANE Select	NP_004644.2:p.Pro1130Gln
NM_001146705.2:c.3482C>A	NP_001140177.1:p.Pro1161Gln