Canonical Allele Identifier: CA414844352

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869857C>A (hg19) ; chrY:g.19707971C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707971C>A , CM000686.2:g.19707971C>A	GRCh38
NC_000024.9:g.21869857C>A , CM000686.1:g.21869857C>A	GRCh37
NC_000024.8:g.20329245C>A	NCBI36
NG_032920.1:g.41969G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.3362G>T MANE Select	ENSP00000322408.4:p.Gly1121Val
ENST00000317961.8:c.3362G>T	ENSP00000322408.4:p.Gly1121Val
ENST00000382806.6:c.3191G>T	ENSP00000372256.2:p.Gly1064Val
ENST00000415360.1:c.278G>T	ENSP00000389433.1:p.Gly93Val
ENST00000440077.5:c.3239G>T	ENSP00000398543.1:p.Gly1080Val
ENST00000469599.6:n.1960G>T
ENST00000492117.1:n.3254G>T
ENST00000541639.5:c.3455G>T	ENSP00000444293.1:p.Gly1152Val
NM_001146705.1:c.3455G>T	NP_001140177.1:p.Gly1152Val
NM_001146706.1:c.3191G>T	NP_001140178.1:p.Gly1064Val
NM_004653.4:c.3362G>T	NP_004644.2:p.Gly1121Val
XM_005262560.1:c.3227G>T	XP_005262617.1:p.Gly1076Val
XM_005262561.1:c.3131G>T	XP_005262618.1:p.Gly1044Val
XM_011531468.1:c.3284G>T	XP_011529770.1:p.Gly1095Val
XR_244571.2:n.3650G>T
XR_430568.2:n.3984G>T
XM_005262560.3:c.3227G>T	XP_005262617.1:p.Gly1076Val
XM_005262561.3:c.3131G>T	XP_005262618.1:p.Gly1044Val
XM_011531468.3:c.3284G>T	XP_011529770.1:p.Gly1095Val
XM_024452495.1:c.1352G>T	XP_024308263.1:p.Gly451Val
XM_024452496.1:c.1118G>T	XP_024308264.1:p.Gly373Val
XR_001756009.2:n.4100G>T
XR_001756010.2:n.4100G>T
XR_001756011.2:n.3965G>T
XR_001756012.2:n.4113G>T
XR_001756013.2:n.3431G>T
XR_002958832.1:n.3532G>T
XR_002958834.1:n.3756G>T
XR_002958835.1:n.3639G>T
XR_002958836.1:n.4322G>T
XR_002958837.1:n.4129G>T
XR_244571.4:n.3649G>T
XR_430568.4:n.3983G>T
NM_001146706.2:c.3191G>T	NP_001140178.1:p.Gly1064Val
NM_004653.5:c.3362G>T MANE Select	NP_004644.2:p.Gly1121Val
NM_001146705.2:c.3455G>T	NP_001140177.1:p.Gly1152Val