Canonical Allele Identifier: CA337441001
Gene: KDM5D HGNC NCBI

Linked Data

dbSNP Id: rs2032638
gnomAD v3: Y-19732561-C-T
gnomAD v4: Y-19732561-C-T
MyVariant Identifiers: chrY:g.21894447C>T (hg19) chrY:g.19732561C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19732561C>T , CM000686.2:g.19732561C>T GRCh38
NC_000024.9:g.21894447C>T , CM000686.1:g.21894447C>T GRCh37
NC_000024.8:g.20353835C>T NCBI36
NG_032920.1:g.17379G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317961.9:c.1092+23G>A MANE Select ENSP00000322408.4:n.1092+23G>A
ENST00000317961.8:c.1092+23G>A ENSP00000322408.4:n.1092+23G>A
ENST00000382806.6:c.921+23G>A ENSP00000372256.2:n.921+23G>A
ENST00000440077.5:c.969+23G>A ENSP00000398543.1:n.969+23G>A
ENST00000447300.1:c.957+23G>A ENSP00000416377.1:n.957+23G>A
ENST00000541639.5:c.1092+23G>A ENSP00000444293.1:n.1092+23G>A
NM_001146705.1:c.1092+23G>A NP_001140177.1:n.1092+23G>A
NM_001146706.1:c.921+23G>A NP_001140178.1:n.921+23G>A
NM_004653.4:c.1092+23G>A NP_004644.2:n.1092+23G>A
XM_005262560.1:c.957+23G>A XP_005262617.1:n.957+23G>A
XM_005262561.1:c.1092+23G>A XP_005262618.1:n.1092+23G>A
XM_005262562.2:c.1092+23G>A XP_005262619.1:n.1092+23G>A
XM_011531468.1:c.1092+23G>A XP_011529770.1:n.1092+23G>A
XR_244571.2:n.1380+23G>A
XR_430568.2:n.1380+23G>A
XR_938609.1:n.1380+23G>A
XR_938610.1:n.1380+23G>A
XM_005262560.3:c.957+23G>A XP_005262617.1:n.957+23G>A
XM_005262561.3:c.1092+23G>A XP_005262618.1:n.1092+23G>A
XM_011531468.3:c.1092+23G>A XP_011529770.1:n.1092+23G>A
XM_024452495.1:c.-1026+23G>A XP_024308263.1:n.-1026+23G>A
XR_001756009.2:n.1379+23G>A
XR_001756010.2:n.1379+23G>A
XR_001756011.2:n.1244+23G>A
XR_001756012.2:n.1379+23G>A
XR_001756013.2:n.1379+23G>A
XR_002958832.1:n.1379+23G>A
XR_002958833.1:n.1379+23G>A
XR_002958834.1:n.1379+23G>A
XR_002958835.1:n.1379+23G>A
XR_002958836.1:n.1379+23G>A
XR_002958837.1:n.1379+23G>A
XR_244571.4:n.1379+23G>A
XR_430568.4:n.1379+23G>A
NM_001146706.2:c.921+23G>A NP_001140178.1:n.921+23G>A
NM_004653.5:c.1092+23G>A MANE Select NP_004644.2:n.1092+23G>A
NM_001146705.2:c.1092+23G>A NP_001140177.1:n.1092+23G>A
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