Canonical Allele Identifier: CA390255576

Gene: GPHN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.66824549C>T , CM000676.2:g.66824549C>T	GRCh38
NC_000014.8:g.67291267C>T , CM000676.1:g.67291267C>T	GRCh37
NC_000014.7:g.66361020C>T	NCBI36
NG_008875.1:g.322143C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020806.5:c.277C>T MANE Select	NP_065857.1:p.Arg93Ter
ENST00000478722.6:c.277C>T MANE Select	ENSP00000417901.1:p.Arg93Ter
NM_001024218.1:c.277C>T	NP_001019389.1:p.Arg93Ter
NM_001024218.2:c.277C>T	NP_001019389.1:p.Arg93Ter
NM_001377514.1:c.277C>T	NP_001364443.1:p.Arg93Ter
NM_001377515.1:c.277C>T	NP_001364444.1:p.Arg93Ter
NM_001377516.1:c.277C>T	NP_001364445.1:p.Arg93Ter
NM_001377517.1:c.277C>T	NP_001364446.1:p.Arg93Ter
NM_001377518.1:c.277C>T	NP_001364447.1:p.Arg93Ter
NM_001377519.1:c.277C>T	NP_001364448.1:p.Arg93Ter
NM_020806.4:c.277C>T	NP_065857.1:p.Arg93Ter
ENST00000315266.9:c.277C>T	ENSP00000312771.5:p.Arg93Ter
ENST00000459628.5:c.202-18129C>T	ENSP00000452220.1:n.202-18129C>T
ENST00000478722.5:c.277C>T	ENSP00000417901.1:p.Arg93Ter
ENST00000543237.5:c.277C>T	ENSP00000438404.1:p.Arg93Ter
ENST00000544752.6:n.325C>T
ENST00000553936.5:c.*298C>T	ENSP00000451725.1:n.*298C>T
ENST00000555456.1:c.76C>T	ENSP00000450706.1:p.Arg26Ter
ENST00000555668.5:c.*229C>T	ENSP00000451935.1:n.*229C>T
ENST00000556020.1:n.557C>T
ENST00000556633.5:c.*66C>T	ENSP00000451056.1:n.*66C>T
ENST00000557654.5:c.*229C>T	ENSP00000451790.1:n.*229C>T
XM_005267254.2:c.277C>T	XP_005267311.1:p.Arg93Ter
XM_005267254.4:c.277C>T	XP_005267311.1:p.Arg93Ter
XM_011536340.1:c.277C>T	XP_011534642.1:p.Arg93Ter
XM_011536340.3:c.277C>T	XP_011534642.1:p.Arg93Ter
XM_011536342.1:c.277C>T	XP_011534644.1:p.Arg93Ter
XM_011536342.3:c.277C>T	XP_011534644.1:p.Arg93Ter
XM_011536343.1:c.277C>T	XP_011534645.1:p.Arg93Ter
XM_011536343.3:c.277C>T	XP_011534645.1:p.Arg93Ter
XM_011536344.1:c.277C>T	XP_011534646.1:p.Arg93Ter
XM_011536344.3:c.277C>T	XP_011534646.1:p.Arg93Ter
XM_011536345.1:c.277C>T	XP_011534647.1:p.Arg93Ter
XM_011536345.3:c.277C>T	XP_011534647.1:p.Arg93Ter
XM_011536346.1:c.277C>T	XP_011534648.1:p.Arg93Ter
XM_011536346.3:c.277C>T	XP_011534648.1:p.Arg93Ter
XM_011536347.1:c.277C>T	XP_011534649.1:p.Arg93Ter
XM_011536347.2:c.277C>T	XP_011534649.1:p.Arg93Ter
XM_011536349.1:c.277C>T	XP_011534651.1:p.Arg93Ter
XM_017020913.2:c.277C>T	XP_016876402.1:p.Arg93Ter
XM_017020914.2:c.277C>T	XP_016876403.1:p.Arg93Ter
XM_017020915.2:c.277C>T	XP_016876404.1:p.Arg93Ter
XM_017020916.2:c.277C>T	XP_016876405.1:p.Arg93Ter
XM_017020917.2:c.277C>T	XP_016876406.1:p.Arg93Ter
XM_017020918.2:c.277C>T	XP_016876407.1:p.Arg93Ter
XM_017020919.2:c.277C>T	XP_016876408.1:p.Arg93Ter
XM_017020920.2:c.136C>T	XP_016876409.1:p.Arg46Ter
XM_017020921.1:c.-54C>T	XP_016876410.1:n.-54C>T
XM_017020922.1:c.-93C>T	XP_016876411.1:n.-93C>T
XM_017020923.1:c.-54C>T	XP_016876412.1:n.-54C>T
XM_017020924.1:c.-735C>T	XP_016876413.1:n.-735C>T
XM_017020925.2:c.277C>T	XP_016876414.1:p.Arg93Ter
XM_017020926.1:c.-735C>T	XP_016876415.1:n.-735C>T