Canonical Allele Identifier: CA356482510

Gene: ADGRA3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.22438268T>G , CM000666.2:g.22438268T>G	GRCh38
NC_000004.11:g.22439891T>G , CM000666.1:g.22439891T>G	GRCh37
NC_000004.10:g.22048989T>G	NCBI36
NG_032963.1:g.82787A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_145290.4:c.1073A>C MANE Select	NP_660333.2:p.Lys358Thr
ENST00000334304.10:c.1073A>C MANE Select	ENSP00000334952.5:p.Lys358Thr
NM_145290.3:c.1073A>C	NP_660333.2:p.Lys358Thr
ENST00000282943.9:n.698A>C
ENST00000334304.9:c.1073A>C	ENSP00000334952.5:p.Lys358Thr
ENST00000502482.1:c.1073A>C	ENSP00000421006.1:p.Lys358Thr
ENST00000508133.5:c.395A>C	ENSP00000422606.1:p.Lys132Thr
ENST00000514129.5:c.281A>C	ENSP00000425223.1:p.Lys94Thr
XM_005248137.3:c.1073A>C	XP_005248194.1:p.Lys358Thr
XM_005248137.5:c.1073A>C	XP_005248194.1:p.Lys358Thr
XM_011513810.1:c.482A>C	XP_011512112.1:p.Lys161Thr
XM_011513811.1:c.395A>C	XP_011512113.1:p.Lys132Thr
XM_011513811.2:c.395A>C	XP_011512113.1:p.Lys132Thr
XR_001741153.1:n.1347A>C
XR_925316.1:n.1347A>C