Canonical Allele Identifier: CA3207024037
Community Standard Title: NM_020806.5(GPHN):c.1007-883C=
Gene: GPHN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67057766C= , CM000676.2:g.67057766C= GRCh38
NC_000014.8:g.67524483C= , CM000676.1:g.67524483C= GRCh37
NC_000014.7:g.66594236C= NCBI36
NG_008875.1:g.555359C=

Transcript Alleles

HGVS Amino-acid Change
NM_020806.5:c.1007-883C= MANE Select NP_065857.1:n.1007-883C=
ENST00000478722.6:c.1007-883C= MANE Select ENSP00000417901.1:n.1007-883C=
NM_001024218.1:c.908-883C= NP_001019389.1:n.908-883C=
NM_001024218.2:c.908-883C= NP_001019389.1:n.908-883C=
NM_001377514.1:c.1067-883C= NP_001364443.1:n.1067-883C=
NM_001377515.1:c.1037-883C= NP_001364444.1:n.1037-883C=
NM_001377516.1:c.1028-883C= NP_001364445.1:n.1028-883C=
NM_001377517.1:c.980-883C= NP_001364446.1:n.980-883C=
NM_001377518.1:c.965-883C= NP_001364447.1:n.965-883C=
NM_001377519.1:c.947-883C= NP_001364448.1:n.947-883C=
NM_020806.4:c.1007-883C= NP_065857.1:n.1007-883C=
ENST00000315266.9:c.908-883C= ENSP00000312771.5:n.908-883C=
ENST00000459628.5:c.953-883C= ENSP00000452220.1:n.953-883C=
ENST00000478722.5:c.1007-883C= ENSP00000417901.1:n.1007-883C=
ENST00000543237.5:c.1046-883C= ENSP00000438404.1:n.1046-883C=
ENST00000544752.6:n.1055-883C=
ENST00000555456.1:c.764-883C= ENSP00000450706.1:n.764-883C=
XM_005267254.2:c.965-883C= XP_005267311.1:n.965-883C=
XM_005267254.4:c.965-883C= XP_005267311.1:n.965-883C=
XM_011536340.1:c.1175-883C= XP_011534642.1:n.1175-883C=
XM_011536340.3:c.1175-883C= XP_011534642.1:n.1175-883C=
XM_011536342.1:c.1136-883C= XP_011534644.1:n.1136-883C=
XM_011536342.3:c.1136-883C= XP_011534644.1:n.1136-883C=
XM_011536343.1:c.1103-883C= XP_011534645.1:n.1103-883C=
XM_011536343.3:c.1103-883C= XP_011534645.1:n.1103-883C=
XM_011536344.1:c.1076-883C= XP_011534646.1:n.1076-883C=
XM_011536344.3:c.1076-883C= XP_011534646.1:n.1076-883C=
XM_011536345.1:c.1046-883C= XP_011534647.1:n.1046-883C=
XM_011536345.3:c.1046-883C= XP_011534647.1:n.1046-883C=
XM_011536346.1:c.1037-883C= XP_011534648.1:n.1037-883C=
XM_011536346.3:c.1037-883C= XP_011534648.1:n.1037-883C=
XM_011536347.1:c.947-883C= XP_011534649.1:n.947-883C=
XM_011536347.2:c.947-883C= XP_011534649.1:n.947-883C=
XM_011536348.1:c.158-883C= XP_011534650.1:n.158-883C=
XM_017020913.2:c.1166-883C= XP_016876402.1:n.1166-883C=
XM_017020914.2:c.1118-883C= XP_016876403.1:n.1118-883C=
XM_017020915.2:c.1067-883C= XP_016876404.1:n.1067-883C=
XM_017020916.2:c.1028-883C= XP_016876405.1:n.1028-883C=
XM_017020917.2:c.1019-883C= XP_016876406.1:n.1019-883C=
XM_017020918.2:c.1004-883C= XP_016876407.1:n.1004-883C=
XM_017020919.2:c.980-883C= XP_016876408.1:n.980-883C=
XM_017020920.2:c.866-883C= XP_016876409.1:n.866-883C=
XM_017020921.1:c.806-883C= XP_016876410.1:n.806-883C=
XM_017020922.1:c.806-883C= XP_016876411.1:n.806-883C=
XM_017020923.1:c.677-883C= XP_016876412.1:n.677-883C=
XM_017020924.1:c.158-883C= XP_016876413.1:n.158-883C=
XM_017020925.2:c.1175-883C= XP_016876414.1:n.1175-883C=
XM_017020926.1:c.86-883C= XP_016876415.1:n.86-883C=