Canonical Allele Identifier: CA11946745
Gene: PRELID2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145832582C>T , CM000667.2:g.145832582C>T GRCh38
NC_000005.9:g.145212145C>T , CM000667.1:g.145212145C>T GRCh37
NC_000005.8:g.145192338C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000683046.1:c.75+2595G>A MANE Select ENSP00000506938.1:n.75+2595G>A
ENST00000334744.8:c.75+2595G>A ENSP00000335675.4:n.75+2595G>A
ENST00000394450.6:c.-216+2595G>A ENSP00000377965.2:n.-216+2595G>A
ENST00000505416.5:c.75+2595G>A ENSP00000424730.1:n.75+2595G>A
ENST00000511435.1:c.75+2595G>A ENSP00000422789.1:n.75+2595G>A
ENST00000515475.1:n.193+2595G>A
NM_138492.5:c.-216+2595G>A NP_612501.3:n.-216+2595G>A
NM_182960.3:c.75+2595G>A NP_892005.1:n.75+2595G>A
NM_205846.2:c.75+2595G>A NP_995318.1:n.75+2595G>A
XM_011537561.1:c.75+2595G>A XP_011535863.1:n.75+2595G>A
XM_011537562.1:c.75+2595G>A XP_011535864.1:n.75+2595G>A
XM_011537563.1:c.75+2595G>A XP_011535865.1:n.75+2595G>A
XM_011537564.1:c.75+2595G>A XP_011535866.1:n.75+2595G>A
XM_011537565.1:c.-216+2595G>A XP_011535867.1:n.-216+2595G>A
XM_011537566.1:c.75+2595G>A XP_011535868.1:n.75+2595G>A
XR_944308.1:n.193+2595G>A
XM_017009127.1:c.75+2595G>A XP_016864616.1:n.75+2595G>A
XM_017009128.1:c.75+2595G>A XP_016864617.1:n.75+2595G>A
XM_017009129.1:c.75+2595G>A XP_016864618.1:n.75+2595G>A
XM_017009130.1:c.75+2595G>A XP_016864619.1:n.75+2595G>A
XM_017009131.1:c.75+2595G>A XP_016864620.1:n.75+2595G>A
XM_017009132.1:c.75+2595G>A XP_016864621.1:n.75+2595G>A
XM_017009133.1:c.75+2595G>A XP_016864622.1:n.75+2595G>A
XM_017009134.1:c.75+2595G>A XP_016864623.1:n.75+2595G>A
XM_017009135.1:c.75+2595G>A XP_016864624.1:n.75+2595G>A
XR_001742019.1:n.193+2595G>A
XR_001742021.1:n.193+2595G>A
XR_001742022.2:n.178+2595G>A
XR_001742024.2:n.173+2595G>A
XR_001742025.1:n.193+2595G>A
NM_138492.6:c.-216+2595G>A NP_612501.3:n.-216+2595G>A
NM_182960.4:c.75+2595G>A NP_892005.1:n.75+2595G>A
NM_205846.3:c.75+2595G>A MANE Select NP_995318.1:n.75+2595G>A
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