Canonical Allele Identifier: CA98204419

Gene: ADGRL3

Linked Data

• dbSNP Id: rs147377039
• gnomAD v2: 4-62067899-G-T
• gnomAD v3: 4-61202181-G-T
• gnomAD v4: 4-61202181-G-T
• MyVariant Identifiers: chr4:g.62067899G>T (hg19) ; chr4:g.61202181G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.61202181G>T , CM000666.2:g.61202181G>T	GRCh38
NC_000004.11:g.62067899G>T , CM000666.1:g.62067899G>T	GRCh37
NC_000004.10:g.61750494G>T	NCBI36
NG_033950.2:g.5926G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683033.1:c.-240+416G>T MANE Select	ENSP00000507980.1:n.-240+416G>T
ENST00000509779.5:n.102+416G>T
ENST00000512091.6:c.-240+416G>T	ENSP00000423388.1:n.-240+416G>T
ENST00000514591.5:c.-290G>T	ENSP00000422533.1:n.-290G>T
NM_001322246.1:c.-240+416G>T	NP_001309175.1:n.-240+416G>T
NM_001322402.1:c.-240+416G>T	NP_001309331.1:n.-240+416G>T
NM_015236.5:c.-240+416G>T	NP_056051.2:n.-240+416G>T
NM_001322246.2:c.-240+416G>T	NP_001309175.1:n.-240+416G>T
NM_001322402.2:c.-240+416G>T	NP_001309331.1:n.-240+416G>T
NM_001371342.1:c.-734G>T	NP_001358271.1:n.-734G>T
NM_001371343.1:c.-240+416G>T	NP_001358272.1:n.-240+416G>T
NM_001371344.1:c.-174+416G>T	NP_001358273.1:n.-174+416G>T
NM_001371345.1:c.-174+416G>T	NP_001358274.1:n.-174+416G>T
NM_001371346.1:c.-174+416G>T	NP_001358275.1:n.-174+416G>T
NM_015236.6:c.-240+416G>T	NP_056051.2:n.-240+416G>T
NM_001322246.3:c.-240+416G>T	NP_001309175.1:n.-240+416G>T
NM_001322402.3:c.-240+416G>T	NP_001309331.1:n.-240+416G>T
NM_001371343.2:c.-240+416G>T	NP_001358272.1:n.-240+416G>T
NM_001371344.2:c.-174+416G>T	NP_001358273.1:n.-174+416G>T
NM_001371345.2:c.-174+416G>T	NP_001358274.1:n.-174+416G>T
NM_001371346.2:c.-174+416G>T	NP_001358275.1:n.-174+416G>T
NM_001387522.1:c.-240+416G>T	NP_001374451.1:n.-240+416G>T
NM_001387523.1:c.-240+416G>T	NP_001374452.1:n.-240+416G>T
NM_001387524.1:c.-240+416G>T	NP_001374453.1:n.-240+416G>T
NM_001387525.1:c.-174+416G>T	NP_001374454.1:n.-174+416G>T
NM_001387526.1:c.-174+416G>T	NP_001374455.1:n.-174+416G>T
NM_001387527.1:c.-174+416G>T	NP_001374456.1:n.-174+416G>T
NM_001387528.1:c.-174+416G>T	NP_001374457.1:n.-174+416G>T
NM_001387529.1:c.-174+416G>T	NP_001374458.1:n.-174+416G>T
NM_001387530.1:c.-734G>T	NP_001374459.1:n.-734G>T
NM_001387531.1:c.-174+416G>T	NP_001374460.1:n.-174+416G>T
NM_001387532.1:c.-800G>T	NP_001374461.1:n.-800G>T
NM_001387533.1:c.-174+416G>T	NP_001374462.1:n.-174+416G>T
NM_001387534.1:c.-240+416G>T	NP_001374463.1:n.-240+416G>T
NM_001387535.1:c.-174+416G>T	NP_001374464.1:n.-174+416G>T
NM_001387536.1:c.-240+416G>T	NP_001374465.1:n.-240+416G>T
NM_001387537.1:c.-174+416G>T	NP_001374466.1:n.-174+416G>T
NM_001387538.1:c.-240+416G>T	NP_001374467.1:n.-240+416G>T
NM_001387539.1:c.-800G>T	NP_001374468.1:n.-800G>T
NM_001387540.1:c.-240+416G>T	NP_001374469.1:n.-240+416G>T
NM_001387541.1:c.-74G>T	NP_001374470.1:n.-74G>T
NM_001387542.1:c.-174+416G>T	NP_001374471.1:n.-174+416G>T
NM_001387543.1:c.-396G>T	NP_001374472.1:n.-396G>T
NM_001387544.1:c.-412+416G>T	NP_001374473.1:n.-412+416G>T
NM_001387545.1:c.-174+416G>T	NP_001374474.1:n.-174+416G>T
NM_001387546.1:c.-174+416G>T	NP_001374475.1:n.-174+416G>T
NM_001387547.1:c.-174+416G>T	NP_001374476.1:n.-174+416G>T
NM_001387548.1:c.-240+416G>T	NP_001374477.1:n.-240+416G>T
NM_001387549.1:c.-174+416G>T	NP_001374478.1:n.-174+416G>T
NM_001387552.1:c.-240+416G>T MANE Select	NP_001374481.1:n.-240+416G>T
NM_015236.7:c.-240+416G>T	NP_056051.2:n.-240+416G>T