Canonical Allele Identifier: CA2180476220

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665049_58665050delinsCA , CM000677.2:g.58665049_58665050delinsCA	GRCh38
NC_000015.9:g.58957248_58957249delinsCA , CM000677.1:g.58957248_58957249delinsCA	GRCh37
NC_000015.8:g.56744540_56744541delinsCA	NCBI36
NG_033876.1:g.89929_89930delinsTG
NG_033876.2:g.89658_89659delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.585+47_585+48delinsTG MANE Select	ENSP00000260408.3:n.585+47_585+48delinsTG
ENST00000260408.7:c.585+47_585+48delinsTG	ENSP00000260408.3:n.585+47_585+48delinsTG
ENST00000396136.6:c.411+47_411+48delinsTG
ENST00000402627.5:c.56-24220_56-24219delinsTG	ENSP00000386056.1:n.56-24220_56-24219delinsTG
ENST00000558733.5:n.821+47_821+48delinsTG
ENST00000559053.1:c.56-24220_56-24219delinsTG	ENSP00000453952.1:n.56-24220_56-24219delinsTG
ENST00000561288.1:c.56-67532_56-67531delinsTG	ENSP00000452639.1:n.56-67532_56-67531delinsTG
NM_001110.3:c.585+47_585+48delinsTG	NP_001101.1:n.585+47_585+48delinsTG
XM_005254117.2:c.585+47_585+48delinsTG	XP_005254174.1:n.585+47_585+48delinsTG
NM_001320570.1:c.585+47_585+48delinsTG	NP_001307499.1:n.585+47_585+48delinsTG
XM_024449818.1:c.363+47_363+48delinsTG	XP_024305586.1:n.363+47_363+48delinsTG
NM_001110.4:c.585+47_585+48delinsTG MANE Select	NP_001101.1:n.585+47_585+48delinsTG
NM_001320570.2:c.585+47_585+48delinsTG	NP_001307499.1:n.585+47_585+48delinsTG