Canonical Allele Identifier: CA414844805

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869958C>T (hg19) ; chrY:g.19708072C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708072C>T , CM000686.2:g.19708072C>T	GRCh38
NC_000024.9:g.21869958C>T , CM000686.1:g.21869958C>T	GRCh37
NC_000024.8:g.20329346C>T	NCBI36
NG_032920.1:g.41868G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3262-1G>A MANE Select	ENSP00000322408.4:n.3262-1G>A
ENST00000317961.8:c.3262-1G>A	ENSP00000322408.4:n.3262-1G>A
ENST00000382806.6:c.3091-1G>A	ENSP00000372256.2:n.3091-1G>A
ENST00000415360.1:c.178-1G>A	ENSP00000389433.1:n.178-1G>A
ENST00000440077.5:c.3139-1G>A	ENSP00000398543.1:n.3139-1G>A
ENST00000469599.6:n.1860-1G>A
ENST00000492117.1:n.3154-1G>A
ENST00000541639.5:c.3355-1G>A	ENSP00000444293.1:n.3355-1G>A
NM_001146705.1:c.3355-1G>A	NP_001140177.1:n.3355-1G>A
NM_001146706.1:c.3091-1G>A	NP_001140178.1:n.3091-1G>A
NM_004653.4:c.3262-1G>A	NP_004644.2:n.3262-1G>A
XM_005262560.1:c.3127-1G>A	XP_005262617.1:n.3127-1G>A
XM_005262561.1:c.3031-1G>A	XP_005262618.1:n.3031-1G>A
XM_011531468.1:c.3184-1G>A	XP_011529770.1:n.3184-1G>A
XR_244571.2:n.3550-1G>A
XR_430568.2:n.3884-1G>A
XM_005262560.3:c.3127-1G>A	XP_005262617.1:n.3127-1G>A
XM_005262561.3:c.3031-1G>A	XP_005262618.1:n.3031-1G>A
XM_011531468.3:c.3184-1G>A	XP_011529770.1:n.3184-1G>A
XM_024452495.1:c.1252-1G>A	XP_024308263.1:n.1252-1G>A
XM_024452496.1:c.1018-1G>A	XP_024308264.1:n.1018-1G>A
XR_001756009.2:n.4000-1G>A
XR_001756010.2:n.4000-1G>A
XR_001756011.2:n.3865-1G>A
XR_001756012.2:n.4013-1G>A
XR_001756013.2:n.3331-1G>A
XR_002958832.1:n.3432-1G>A
XR_002958834.1:n.3656-1G>A
XR_002958835.1:n.3539-1G>A
XR_002958836.1:n.4222-1G>A
XR_002958837.1:n.4029-1G>A
XR_244571.4:n.3549-1G>A
XR_430568.4:n.3883-1G>A
NM_001146706.2:c.3091-1G>A	NP_001140178.1:n.3091-1G>A
NM_004653.5:c.3262-1G>A MANE Select	NP_004644.2:n.3262-1G>A
NM_001146705.2:c.3355-1G>A	NP_001140177.1:n.3355-1G>A