Canonical Allele Identifier: CA414844226

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869818A>T (hg19) ; chrY:g.19707932A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707932A>T , CM000686.2:g.19707932A>T	GRCh38
NC_000024.9:g.21869818A>T , CM000686.1:g.21869818A>T	GRCh37
NC_000024.8:g.20329206A>T	NCBI36
NG_032920.1:g.42008T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.3399+2T>A MANE Select	ENSP00000322408.4:n.3399+2T>A
ENST00000317961.8:c.3399+2T>A	ENSP00000322408.4:n.3399+2T>A
ENST00000382806.6:c.3228+2T>A	ENSP00000372256.2:n.3228+2T>A
ENST00000415360.1:c.315+2T>A	ENSP00000389433.1:n.315+2T>A
ENST00000440077.5:c.3276+2T>A	ENSP00000398543.1:n.3276+2T>A
ENST00000469599.6:n.1997+2T>A
ENST00000492117.1:n.3291+2T>A
ENST00000541639.5:c.3492+2T>A	ENSP00000444293.1:n.3492+2T>A
NM_001146705.1:c.3492+2T>A	NP_001140177.1:n.3492+2T>A
NM_001146706.1:c.3228+2T>A	NP_001140178.1:n.3228+2T>A
NM_004653.4:c.3399+2T>A	NP_004644.2:n.3399+2T>A
XM_005262560.1:c.3264+2T>A	XP_005262617.1:n.3264+2T>A
XM_005262561.1:c.3168+2T>A	XP_005262618.1:n.3168+2T>A
XM_011531468.1:c.3321+2T>A	XP_011529770.1:n.3321+2T>A
XR_244571.2:n.3687+2T>A
XR_430568.2:n.4021+2T>A
XM_005262560.3:c.3264+2T>A	XP_005262617.1:n.3264+2T>A
XM_005262561.3:c.3168+2T>A	XP_005262618.1:n.3168+2T>A
XM_011531468.3:c.3321+2T>A	XP_011529770.1:n.3321+2T>A
XM_024452495.1:c.1389+2T>A	XP_024308263.1:n.1389+2T>A
XM_024452496.1:c.1155+2T>A	XP_024308264.1:n.1155+2T>A
XR_001756009.2:n.4137+2T>A
XR_001756010.2:n.4137+2T>A
XR_001756011.2:n.4002+2T>A
XR_001756012.2:n.4150+2T>A
XR_001756013.2:n.3468+2T>A
XR_002958832.1:n.3569+2T>A
XR_002958834.1:n.3793+2T>A
XR_002958835.1:n.3676+2T>A
XR_002958836.1:n.4359+2T>A
XR_002958837.1:n.4166+2T>A
XR_244571.4:n.3686+2T>A
XR_430568.4:n.4020+2T>A
NM_001146706.2:c.3228+2T>A	NP_001140178.1:n.3228+2T>A
NM_004653.5:c.3399+2T>A MANE Select	NP_004644.2:n.3399+2T>A
NM_001146705.2:c.3492+2T>A	NP_001140177.1:n.3492+2T>A