Canonical Allele Identifier: CA915949281

Gene: ADGRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57620144A>T , CM000678.2:g.57620144A>T	GRCh38
NC_000016.9:g.57654056A>T , CM000678.1:g.57654056A>T	GRCh37
NC_000016.8:g.56211557A>T	NCBI36
NG_011643.1:g.5147A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561872.5:n.91+8A>T
ENST00000561988.5:c.-158+8A>T	ENSP00000456238.1:n.-158+8A>T
ENST00000562003.5:c.-36+8A>T	ENSP00000454607.1:n.-36+8A>T
ENST00000562101.5:n.91+8A>T
ENST00000562673.5:n.142+263A>T
ENST00000563548.5:c.-154+8A>T	ENSP00000454263.1:n.-154+8A>T
ENST00000564907.5:c.-36+263A>T	ENSP00000455245.1:n.-36+263A>T
ENST00000564912.5:n.144+263A>T
ENST00000565314.5:c.-36+263A>T	ENSP00000456469.1:n.-36+263A>T
ENST00000565587.5:c.-154+9232A>T	ENSP00000456781.1:n.-154+9232A>T
ENST00000566778.5:c.-154+8A>T	ENSP00000456796.1:n.-154+8A>T
ENST00000567553.5:c.-154+263A>T	ENSP00000455812.1:n.-154+263A>T
ENST00000567835.5:c.-154+8A>T	ENSP00000456794.1:n.-154+8A>T
ENST00000568791.5:c.-158+263A>T	ENSP00000454321.1:n.-158+263A>T
ENST00000568908.5:c.-154+8A>T	ENSP00000457456.1:n.-154+8A>T
ENST00000568909.5:c.-36+8A>T	ENSP00000455215.1:n.-36+8A>T
ENST00000569372.5:c.-191+8A>T	ENSP00000457979.1:n.-191+8A>T
ENST00000570044.5:c.-154+263A>T	ENSP00000456166.1:n.-154+263A>T
NM_001145770.2:c.-154+8A>T	NP_001139242.1:n.-154+8A>T
NM_001290142.1:c.-154+263A>T	NP_001277071.1:n.-154+263A>T
NM_001290143.1:c.-518+263A>T	NP_001277072.1:n.-518+263A>T
NM_005682.6:c.-154+8A>T	NP_005673.3:n.-154+8A>T
XM_005256240.3:c.-36+8A>T	XP_005256297.1:n.-36+8A>T
XM_005256242.3:c.-36+263A>T	XP_005256299.1:n.-36+263A>T
XM_005256249.2:c.-36+8A>T	XP_005256306.1:n.-36+8A>T
XM_005256251.3:c.-36+263A>T	XP_005256308.1:n.-36+263A>T
XM_006721339.2:c.-154+8A>T	XP_006721402.1:n.-154+8A>T
XM_006721340.2:c.-154+263A>T	XP_006721403.1:n.-154+263A>T
XM_006721343.2:c.-154+263A>T	XP_006721406.1:n.-154+263A>T
XM_006721345.2:c.-191+8A>T	XP_006721408.1:n.-191+8A>T
XM_011523463.1:c.-158+8A>T	XP_011521765.1:n.-158+8A>T
XM_011523465.1:c.-158+263A>T	XP_011521767.1:n.-158+263A>T
XM_005256240.4:c.-36+8A>T	XP_005256297.1:n.-36+8A>T
XM_005256242.4:c.-36+263A>T	XP_005256299.1:n.-36+263A>T
XM_005256249.3:c.-36+8A>T	XP_005256306.1:n.-36+8A>T
XM_005256251.4:c.-36+263A>T	XP_005256308.1:n.-36+263A>T
XM_006721339.4:c.-154+8A>T	XP_006721402.1:n.-154+8A>T
XM_006721340.3:c.-154+263A>T	XP_006721403.1:n.-154+263A>T
XM_006721343.3:c.-154+263A>T	XP_006721406.1:n.-154+263A>T
XM_006721345.3:c.-191+8A>T	XP_006721408.1:n.-191+8A>T
XM_011523463.2:c.-158+8A>T	XP_011521765.1:n.-158+8A>T
XM_011523465.2:c.-158+263A>T	XP_011521767.1:n.-158+263A>T
NM_001145770.3:c.-154+8A>T	NP_001139242.1:n.-154+8A>T
NM_001290142.2:c.-154+263A>T	NP_001277071.1:n.-154+263A>T
NM_001290143.2:c.-518+263A>T	NP_001277072.1:n.-518+263A>T
NM_001370428.1:c.-154+263A>T	NP_001357357.1:n.-154+263A>T
NM_001370430.1:c.-36+263A>T	NP_001357359.1:n.-36+263A>T
NM_001370431.1:c.-158+8A>T	NP_001357360.1:n.-158+8A>T
NM_001370432.1:c.-36+8A>T	NP_001357361.1:n.-36+8A>T
NM_001370433.1:c.-36+8A>T	NP_001357362.1:n.-36+8A>T
NM_001370434.1:c.-154+8A>T	NP_001357363.1:n.-154+8A>T
NM_001370435.1:c.-36+283A>T	NP_001357364.1:n.-36+283A>T
NM_001370436.1:c.-154+263A>T	NP_001357365.1:n.-154+263A>T
NM_001370437.1:c.-158+8A>T	NP_001357366.1:n.-158+8A>T
NM_001370438.1:c.-36+263A>T	NP_001357367.1:n.-36+263A>T
NM_001370439.1:c.-36+8A>T	NP_001357368.1:n.-36+8A>T
NM_001370440.1:c.-158+263A>T	NP_001357369.1:n.-158+263A>T
NM_001370441.1:c.-36+8A>T	NP_001357370.1:n.-36+8A>T
NM_001370442.1:c.-154+8A>T	NP_001357371.1:n.-154+8A>T
NM_001370451.1:c.-636+263A>T	NP_001357380.1:n.-636+263A>T
NM_001370453.1:c.-720+8A>T	NP_001357382.1:n.-720+8A>T
NM_005682.7:c.-154+8A>T	NP_005673.3:n.-154+8A>T