Canonical Allele Identifier: CA414844040

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869572T>A (hg19) ; chrY:g.19707686T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707686T>A , CM000686.2:g.19707686T>A	GRCh38
NC_000024.9:g.21869572T>A , CM000686.1:g.21869572T>A	GRCh37
NC_000024.8:g.20328960T>A	NCBI36
NG_032920.1:g.42254A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3460A>T MANE Select	ENSP00000322408.4:p.Thr1154Ser
ENST00000317961.8:c.3460A>T	ENSP00000322408.4:p.Thr1154Ser
ENST00000382806.6:c.3289A>T	ENSP00000372256.2:p.Thr1097Ser
ENST00000415360.1:c.376A>T	ENSP00000389433.1:p.Thr126Ser
ENST00000440077.5:c.3337A>T	ENSP00000398543.1:p.Thr1113Ser
ENST00000469599.6:n.2058A>T
ENST00000492117.1:n.3352A>T
ENST00000541639.5:c.3553A>T	ENSP00000444293.1:p.Thr1185Ser
NM_001146705.1:c.3553A>T	NP_001140177.1:p.Thr1185Ser
NM_001146706.1:c.3289A>T	NP_001140178.1:p.Thr1097Ser
NM_004653.4:c.3460A>T	NP_004644.2:p.Thr1154Ser
XM_005262560.1:c.3325A>T	XP_005262617.1:p.Thr1109Ser
XM_005262561.1:c.3229A>T	XP_005262618.1:p.Thr1077Ser
XM_011531468.1:c.3382A>T	XP_011529770.1:p.Thr1128Ser
XR_244571.2:n.3748A>T
XR_430568.2:n.4082A>T
XM_005262560.3:c.3325A>T	XP_005262617.1:p.Thr1109Ser
XM_005262561.3:c.3229A>T	XP_005262618.1:p.Thr1077Ser
XM_011531468.3:c.3382A>T	XP_011529770.1:p.Thr1128Ser
XM_024452495.1:c.1450A>T	XP_024308263.1:p.Thr484Ser
XM_024452496.1:c.1216A>T	XP_024308264.1:p.Thr406Ser
XR_001756009.2:n.4198A>T
XR_001756010.2:n.4198A>T
XR_001756011.2:n.4063A>T
XR_001756012.2:n.4211A>T
XR_001756013.2:n.3529A>T
XR_002958832.1:n.3630A>T
XR_002958834.1:n.3854A>T
XR_002958835.1:n.3737A>T
XR_002958836.1:n.4420A>T
XR_002958837.1:n.4227A>T
XR_244571.4:n.3747A>T
XR_430568.4:n.4081A>T
NM_001146706.2:c.3289A>T	NP_001140178.1:p.Thr1097Ser
NM_004653.5:c.3460A>T MANE Select	NP_004644.2:p.Thr1154Ser
NM_001146705.2:c.3553A>T	NP_001140177.1:p.Thr1185Ser