Canonical Allele Identifier: CA15454820
Gene: PPIL6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109420812G>A , CM000668.2:g.109420812G>A GRCh38
NC_000006.11:g.109742015G>A , CM000668.1:g.109742015G>A GRCh37
NC_000006.10:g.109848708G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521072.7:c.632-1569C>T MANE Select ENSP00000427929.1:n.632-1569C>T
ENST00000417394.6:c.503-1569C>T ENSP00000411731.2:n.503-1569C>T
ENST00000424445.6:c.536-1569C>T ENSP00000407731.2:n.536-1569C>T
ENST00000440797.6:c.632-1569C>T ENSP00000392257.2:n.632-1569C>T
ENST00000447468.7:c.632-1569C>T ENSP00000389292.3:n.632-1569C>T
ENST00000518648.1:c.369-1569C>T
ENST00000520723.5:c.450-1569C>T
ENST00000521072.6:c.632-1569C>T ENSP00000427929.1:n.632-1569C>T
ENST00000524031.1:n.357-1569C>T
NM_001111298.2:c.632-1569C>T NP_001104768.2:n.632-1569C>T
NM_001286360.1:c.536-1569C>T NP_001273289.1:n.536-1569C>T
NM_001286361.1:c.536-1569C>T NP_001273290.1:n.536-1569C>T
NM_173672.4:c.632-1569C>T NP_775943.1:n.632-1569C>T
NR_104429.1:n.1213-1569C>T
XM_011535764.1:c.569-1569C>T XP_011534066.1:n.569-1569C>T
XM_011535765.1:c.536-1569C>T XP_011534067.1:n.536-1569C>T
XM_011535766.1:c.632-1569C>T XP_011534068.1:n.632-1569C>T
XM_011535767.1:c.632-1569C>T XP_011534069.1:n.632-1569C>T
XM_011535768.1:c.443-1569C>T XP_011534070.1:n.443-1569C>T
XM_011535769.1:c.632-1569C>T XP_011534071.1:n.632-1569C>T
XM_011535765.3:c.536-1569C>T XP_011534067.1:n.536-1569C>T
XM_011535766.3:c.632-1569C>T XP_011534068.1:n.632-1569C>T
XM_011535767.3:c.632-1569C>T XP_011534069.1:n.632-1569C>T
XM_011535769.2:c.632-1569C>T XP_011534071.1:n.632-1569C>T
XM_017010774.1:c.632-1569C>T XP_016866263.1:n.632-1569C>T
XM_024446407.1:c.536-1569C>T XP_024302175.1:n.536-1569C>T
NM_173672.5:c.632-1569C>T MANE Select NP_775943.1:n.632-1569C>T
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