Canonical Allele Identifier: CA414844038

Gene: KDM5D

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3460A>C MANE Select	ENSP00000322408.4:p.Thr1154Pro
ENST00000317961.8:c.3460A>C	ENSP00000322408.4:p.Thr1154Pro
ENST00000382806.6:c.3289A>C	ENSP00000372256.2:p.Thr1097Pro
ENST00000415360.1:c.376A>C	ENSP00000389433.1:p.Thr126Pro
ENST00000440077.5:c.3337A>C	ENSP00000398543.1:p.Thr1113Pro
ENST00000469599.6:n.2058A>C
ENST00000492117.1:n.3352A>C
ENST00000541639.5:c.3553A>C	ENSP00000444293.1:p.Thr1185Pro
NM_001146705.1:c.3553A>C	NP_001140177.1:p.Thr1185Pro
NM_001146706.1:c.3289A>C	NP_001140178.1:p.Thr1097Pro
NM_004653.4:c.3460A>C	NP_004644.2:p.Thr1154Pro
XM_005262560.1:c.3325A>C	XP_005262617.1:p.Thr1109Pro
XM_005262561.1:c.3229A>C	XP_005262618.1:p.Thr1077Pro
XM_011531468.1:c.3382A>C	XP_011529770.1:p.Thr1128Pro
XR_244571.2:n.3748A>C
XR_430568.2:n.4082A>C
XM_005262560.3:c.3325A>C	XP_005262617.1:p.Thr1109Pro
XM_005262561.3:c.3229A>C	XP_005262618.1:p.Thr1077Pro
XM_011531468.3:c.3382A>C	XP_011529770.1:p.Thr1128Pro
XM_024452495.1:c.1450A>C	XP_024308263.1:p.Thr484Pro
XM_024452496.1:c.1216A>C	XP_024308264.1:p.Thr406Pro
XR_001756009.2:n.4198A>C
XR_001756010.2:n.4198A>C
XR_001756011.2:n.4063A>C
XR_001756012.2:n.4211A>C
XR_001756013.2:n.3529A>C
XR_002958832.1:n.3630A>C
XR_002958834.1:n.3854A>C
XR_002958835.1:n.3737A>C
XR_002958836.1:n.4420A>C
XR_002958837.1:n.4227A>C
XR_244571.4:n.3747A>C
XR_430568.4:n.4081A>C
NM_001146706.2:c.3289A>C	NP_001140178.1:p.Thr1097Pro
NM_004653.5:c.3460A>C MANE Select	NP_004644.2:p.Thr1154Pro
NM_001146705.2:c.3553A>C	NP_001140177.1:p.Thr1185Pro