Canonical Allele Identifier: CA414840008

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21867958C>A (hg19) ; chrY:g.19706072C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706072C>A , CM000686.2:g.19706072C>A	GRCh38
NC_000024.9:g.21867958C>A , CM000686.1:g.21867958C>A	GRCh37
NC_000024.8:g.20327346C>A	NCBI36
NG_032920.1:g.43868G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4543G>T MANE Select	ENSP00000322408.4:p.Asp1515Tyr
ENST00000317961.8:c.4543G>T	ENSP00000322408.4:p.Asp1515Tyr
ENST00000382806.6:c.4372G>T	ENSP00000372256.2:p.Asp1458Tyr
ENST00000440077.5:c.4420G>T	ENSP00000398543.1:p.Asp1474Tyr
ENST00000469599.6:n.3294G>T
ENST00000492117.1:n.4588G>T
ENST00000541639.5:c.4636G>T	ENSP00000444293.1:p.Asp1546Tyr
NM_001146705.1:c.4636G>T	NP_001140177.1:p.Asp1546Tyr
NM_001146706.1:c.4372G>T	NP_001140178.1:p.Asp1458Tyr
NM_004653.4:c.4543G>T	NP_004644.2:p.Asp1515Tyr
XM_005262560.1:c.4408G>T	XP_005262617.1:p.Asp1470Tyr
XM_005262561.1:c.4312G>T	XP_005262618.1:p.Asp1438Tyr
XM_011531468.1:c.4465G>T	XP_011529770.1:p.Asp1489Tyr
XR_430568.2:n.5318G>T
XM_005262560.3:c.4408G>T	XP_005262617.1:p.Asp1470Tyr
XM_005262561.3:c.4312G>T	XP_005262618.1:p.Asp1438Tyr
XM_011531468.3:c.4465G>T	XP_011529770.1:p.Asp1489Tyr
XM_024452495.1:c.2533G>T	XP_024308263.1:p.Asp845Tyr
XM_024452496.1:c.2299G>T	XP_024308264.1:p.Asp767Tyr
XR_001756009.2:n.5281G>T
XR_001756010.2:n.5249G>T
XR_001756011.2:n.5146G>T
XR_001756012.2:n.5294G>T
XR_001756013.2:n.4612G>T
XR_002958832.1:n.4866G>T
XR_002958834.1:n.4937G>T
XR_002958835.1:n.4820G>T
XR_002958836.1:n.5471G>T
XR_002958837.1:n.5278G>T
XR_244571.4:n.4798G>T
XR_430568.4:n.5317G>T
NM_001146706.2:c.4372G>T	NP_001140178.1:p.Asp1458Tyr
NM_004653.5:c.4543G>T MANE Select	NP_004644.2:p.Asp1515Tyr
NM_001146705.2:c.4636G>T	NP_001140177.1:p.Asp1546Tyr