Canonical Allele Identifier: CA398088290

Gene: GAS7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.9926735A>G , CM000679.2:g.9926735A>G	GRCh38
NC_000017.10:g.9830052A>G , CM000679.1:g.9830052A>G	GRCh37
NC_000017.9:g.9770777A>G	NCBI36
NG_029502.1:g.276817T>C
NG_029502.2:g.276817T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_201433.2:c.920T>C MANE Select	NP_958839.1:p.Phe307Ser
ENST00000432992.7:c.920T>C MANE Select	ENSP00000407552.2:p.Phe307Ser
NM_001130831.1:c.728T>C	NP_001124303.1:p.Phe243Ser
NM_001130831.2:c.728T>C	NP_001124303.1:p.Phe243Ser
NM_003644.2:c.500T>C	NP_003635.2:p.Phe167Ser
NM_003644.3:c.500T>C	NP_003635.2:p.Phe167Ser
NM_201432.1:c.740T>C	NP_958836.1:p.Phe247Ser
NM_201432.2:c.740T>C	NP_958836.1:p.Phe247Ser
NM_201433.1:c.920T>C	NP_958839.1:p.Phe307Ser
ENST00000323816.8:c.740T>C	ENSP00000322608.5:p.Phe247Ser
ENST00000396115.6:c.334-8636T>C	ENSP00000379421.2:n.334-8636T>C
ENST00000432992.6:c.920T>C	ENSP00000407552.2:p.Phe307Ser
ENST00000437099.6:c.728T>C	ENSP00000410108.2:p.Phe243Ser
ENST00000542249.5:c.728T>C	ENSP00000443265.2:p.Phe243Ser
ENST00000578456.1:n.260T>C
ENST00000579158.5:c.728T>C	ENSP00000463527.2:p.Phe243Ser
ENST00000580811.5:n.562T>C
ENST00000580865.5:c.500T>C	ENSP00000463873.1:p.Phe167Ser
ENST00000581871.5:n.474T>C
ENST00000583882.5:c.196-9728T>C	ENSP00000464088.1:n.196-9728T>C
ENST00000585266.5:c.740T>C	ENSP00000464240.2:p.Phe247Ser
XM_005256831.2:c.728T>C	XP_005256888.1:p.Phe243Ser
XM_005256831.4:c.728T>C	XP_005256888.1:p.Phe243Ser
XM_005256832.2:c.728T>C	XP_005256889.1:p.Phe243Ser
XM_005256832.4:c.728T>C	XP_005256889.1:p.Phe243Ser
XM_005256833.2:c.551T>C	XP_005256890.1:p.Phe184Ser
XM_005256833.4:c.551T>C	XP_005256890.1:p.Phe184Ser
XM_005256834.2:c.551T>C	XP_005256891.1:p.Phe184Ser
XM_005256834.4:c.551T>C	XP_005256891.1:p.Phe184Ser
XM_005256835.2:c.551T>C	XP_005256892.1:p.Phe184Ser
XM_005256835.4:c.551T>C	XP_005256892.1:p.Phe184Ser
XM_011524044.1:c.728T>C	XP_011522346.1:p.Phe243Ser
XM_011524044.3:c.728T>C	XP_011522346.1:p.Phe243Ser
XM_017025239.2:c.728T>C	XP_016880728.1:p.Phe243Ser
XM_017025240.2:c.683T>C	XP_016880729.1:p.Phe228Ser
XM_017025241.2:c.659T>C	XP_016880730.1:p.Phe220Ser
XM_017025242.2:c.551T>C	XP_016880731.1:p.Phe184Ser