Canonical Allele Identifier: CA520159525

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868013A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706127A>T , CM000686.2:g.19706127A>T	GRCh38
NC_000024.9:g.21868013A>T , CM000686.1:g.21868013A>T	GRCh37
NC_000024.8:g.20327401A>T	NCBI36
NG_032920.1:g.43813T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4488T>A MANE Select	ENSP00000322408.4:p.Pro1496=
ENST00000317961.8:c.4488T>A	ENSP00000322408.4:p.Pro1496=
ENST00000382806.6:c.4317T>A	ENSP00000372256.2:p.Pro1439=
ENST00000440077.5:c.4365T>A	ENSP00000398543.1:p.Pro1455=
ENST00000469599.6:n.3239T>A
ENST00000492117.1:n.4533T>A
ENST00000541639.5:c.4581T>A	ENSP00000444293.1:p.Pro1527=
NM_001146705.1:c.4581T>A	NP_001140177.1:p.Pro1527=
NM_001146706.1:c.4317T>A	NP_001140178.1:p.Pro1439=
NM_004653.4:c.4488T>A	NP_004644.2:p.Pro1496=
XM_005262560.1:c.4353T>A	XP_005262617.1:p.Pro1451=
XM_005262561.1:c.4257T>A	XP_005262618.1:p.Pro1419=
XM_011531468.1:c.4410T>A	XP_011529770.1:p.Pro1470=
XR_430568.2:n.5263T>A
XM_005262560.3:c.4353T>A	XP_005262617.1:p.Pro1451=
XM_005262561.3:c.4257T>A	XP_005262618.1:p.Pro1419=
XM_011531468.3:c.4410T>A	XP_011529770.1:p.Pro1470=
XM_024452495.1:c.2478T>A	XP_024308263.1:p.Pro826=
XM_024452496.1:c.2244T>A	XP_024308264.1:p.Pro748=
XR_001756009.2:n.5226T>A
XR_001756010.2:n.5194T>A
XR_001756011.2:n.5091T>A
XR_001756012.2:n.5239T>A
XR_001756013.2:n.4557T>A
XR_002958832.1:n.4811T>A
XR_002958834.1:n.4882T>A
XR_002958835.1:n.4765T>A
XR_002958836.1:n.5416T>A
XR_002958837.1:n.5223T>A
XR_244571.4:n.4743T>A
XR_430568.4:n.5262T>A
NM_001146706.2:c.4317T>A	NP_001140178.1:p.Pro1439=
NM_004653.5:c.4488T>A MANE Select	NP_004644.2:p.Pro1496=
NM_001146705.2:c.4581T>A	NP_001140177.1:p.Pro1527=