Canonical Allele Identifier: CA520160834

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869862C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707976C>A , CM000686.2:g.19707976C>A	GRCh38
NC_000024.9:g.21869862C>A , CM000686.1:g.21869862C>A	GRCh37
NC_000024.8:g.20329250C>A	NCBI36
NG_032920.1:g.41964G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.3357G>T MANE Select	ENSP00000322408.4:p.Leu1119=
ENST00000317961.8:c.3357G>T	ENSP00000322408.4:p.Leu1119=
ENST00000382806.6:c.3186G>T	ENSP00000372256.2:p.Leu1062=
ENST00000415360.1:c.273G>T	ENSP00000389433.1:p.Leu91=
ENST00000440077.5:c.3234G>T	ENSP00000398543.1:p.Leu1078=
ENST00000469599.6:n.1955G>T
ENST00000492117.1:n.3249G>T
ENST00000541639.5:c.3450G>T	ENSP00000444293.1:p.Leu1150=
NM_001146705.1:c.3450G>T	NP_001140177.1:p.Leu1150=
NM_001146706.1:c.3186G>T	NP_001140178.1:p.Leu1062=
NM_004653.4:c.3357G>T	NP_004644.2:p.Leu1119=
XM_005262560.1:c.3222G>T	XP_005262617.1:p.Leu1074=
XM_005262561.1:c.3126G>T	XP_005262618.1:p.Leu1042=
XM_011531468.1:c.3279G>T	XP_011529770.1:p.Leu1093=
XR_244571.2:n.3645G>T
XR_430568.2:n.3979G>T
XM_005262560.3:c.3222G>T	XP_005262617.1:p.Leu1074=
XM_005262561.3:c.3126G>T	XP_005262618.1:p.Leu1042=
XM_011531468.3:c.3279G>T	XP_011529770.1:p.Leu1093=
XM_024452495.1:c.1347G>T	XP_024308263.1:p.Leu449=
XM_024452496.1:c.1113G>T	XP_024308264.1:p.Leu371=
XR_001756009.2:n.4095G>T
XR_001756010.2:n.4095G>T
XR_001756011.2:n.3960G>T
XR_001756012.2:n.4108G>T
XR_001756013.2:n.3426G>T
XR_002958832.1:n.3527G>T
XR_002958834.1:n.3751G>T
XR_002958835.1:n.3634G>T
XR_002958836.1:n.4317G>T
XR_002958837.1:n.4124G>T
XR_244571.4:n.3644G>T
XR_430568.4:n.3978G>T
NM_001146706.2:c.3186G>T	NP_001140178.1:p.Leu1062=
NM_004653.5:c.3357G>T MANE Select	NP_004644.2:p.Leu1119=
NM_001146705.2:c.3450G>T	NP_001140177.1:p.Leu1150=