Canonical Allele Identifier: CA414843419

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869404G>C (hg19) ; chrY:g.19707518G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707518G>C , CM000686.2:g.19707518G>C	GRCh38
NC_000024.9:g.21869404G>C , CM000686.1:g.21869404G>C	GRCh37
NC_000024.8:g.20328792G>C	NCBI36
NG_032920.1:g.42422C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3628C>G MANE Select	ENSP00000322408.4:p.Pro1210Ala
ENST00000317961.8:c.3628C>G	ENSP00000322408.4:p.Pro1210Ala
ENST00000382806.6:c.3457C>G	ENSP00000372256.2:p.Pro1153Ala
ENST00000415360.1:c.544C>G	ENSP00000389433.1:p.Pro182Ala
ENST00000440077.5:c.3505C>G	ENSP00000398543.1:p.Pro1169Ala
ENST00000469599.6:n.2226C>G
ENST00000492117.1:n.3520C>G
ENST00000541639.5:c.3721C>G	ENSP00000444293.1:p.Pro1241Ala
NM_001146705.1:c.3721C>G	NP_001140177.1:p.Pro1241Ala
NM_001146706.1:c.3457C>G	NP_001140178.1:p.Pro1153Ala
NM_004653.4:c.3628C>G	NP_004644.2:p.Pro1210Ala
XM_005262560.1:c.3493C>G	XP_005262617.1:p.Pro1165Ala
XM_005262561.1:c.3397C>G	XP_005262618.1:p.Pro1133Ala
XM_011531468.1:c.3550C>G	XP_011529770.1:p.Pro1184Ala
XR_244571.2:n.3916C>G
XR_430568.2:n.4250C>G
XM_005262560.3:c.3493C>G	XP_005262617.1:p.Pro1165Ala
XM_005262561.3:c.3397C>G	XP_005262618.1:p.Pro1133Ala
XM_011531468.3:c.3550C>G	XP_011529770.1:p.Pro1184Ala
XM_024452495.1:c.1618C>G	XP_024308263.1:p.Pro540Ala
XM_024452496.1:c.1384C>G	XP_024308264.1:p.Pro462Ala
XR_001756009.2:n.4366C>G
XR_001756010.2:n.4366C>G
XR_001756011.2:n.4231C>G
XR_001756012.2:n.4379C>G
XR_001756013.2:n.3697C>G
XR_002958832.1:n.3798C>G
XR_002958834.1:n.4022C>G
XR_002958835.1:n.3905C>G
XR_002958836.1:n.4588C>G
XR_002958837.1:n.4395C>G
XR_244571.4:n.3915C>G
XR_430568.4:n.4249C>G
NM_001146706.2:c.3457C>G	NP_001140178.1:p.Pro1153Ala
NM_004653.5:c.3628C>G MANE Select	NP_004644.2:p.Pro1210Ala
NM_001146705.2:c.3721C>G	NP_001140177.1:p.Pro1241Ala