Canonical Allele Identifier: CA414843110
Gene: KDM5D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707428G>A , CM000686.2:g.19707428G>A GRCh38
NC_000024.9:g.21869314G>A , CM000686.1:g.21869314G>A GRCh37
NC_000024.8:g.20328702G>A NCBI36
NG_032920.1:g.42512C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3718C>T MANE Select ENSP00000322408.4:p.Pro1240Ser
ENST00000317961.8:c.3718C>T ENSP00000322408.4:p.Pro1240Ser
ENST00000382806.6:c.3547C>T ENSP00000372256.2:p.Pro1183Ser
ENST00000415360.1:c.634C>T ENSP00000389433.1:p.Pro212Ser
ENST00000440077.5:c.3595C>T ENSP00000398543.1:p.Pro1199Ser
ENST00000469599.6:n.2316C>T
ENST00000492117.1:n.3610C>T
ENST00000541639.5:c.3811C>T ENSP00000444293.1:p.Pro1271Ser
NM_001146705.1:c.3811C>T NP_001140177.1:p.Pro1271Ser
NM_001146706.1:c.3547C>T NP_001140178.1:p.Pro1183Ser
NM_004653.4:c.3718C>T NP_004644.2:p.Pro1240Ser
XM_005262560.1:c.3583C>T XP_005262617.1:p.Pro1195Ser
XM_005262561.1:c.3487C>T XP_005262618.1:p.Pro1163Ser
XM_011531468.1:c.3640C>T XP_011529770.1:p.Pro1214Ser
XR_244571.2:n.4006C>T
XR_430568.2:n.4340C>T
XM_005262560.3:c.3583C>T XP_005262617.1:p.Pro1195Ser
XM_005262561.3:c.3487C>T XP_005262618.1:p.Pro1163Ser
XM_011531468.3:c.3640C>T XP_011529770.1:p.Pro1214Ser
XM_024452495.1:c.1708C>T XP_024308263.1:p.Pro570Ser
XM_024452496.1:c.1474C>T XP_024308264.1:p.Pro492Ser
XR_001756009.2:n.4456C>T
XR_001756010.2:n.4456C>T
XR_001756011.2:n.4321C>T
XR_001756012.2:n.4469C>T
XR_001756013.2:n.3787C>T
XR_002958832.1:n.3888C>T
XR_002958834.1:n.4112C>T
XR_002958835.1:n.3995C>T
XR_002958836.1:n.4678C>T
XR_002958837.1:n.4485C>T
XR_244571.4:n.4005C>T
XR_430568.4:n.4339C>T
NM_001146706.2:c.3547C>T NP_001140178.1:p.Pro1183Ser
NM_004653.5:c.3718C>T MANE Select NP_004644.2:p.Pro1240Ser
NM_001146705.2:c.3811C>T NP_001140177.1:p.Pro1271Ser