Canonical Allele Identifier: CA2586963929

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58679183_58679184insCTCTG , CM000677.2:g.58679183_58679184insCTCTG	GRCh38
NC_000015.9:g.58971382_58971383insCTCTG , CM000677.1:g.58971382_58971383insCTCTG	GRCh37
NC_000015.8:g.56758674_56758675insCTCTG	NCBI36
NG_033876.1:g.75795_75796insCAGAG
NG_033876.2:g.75524_75525insCAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.424_425insCAGAG MANE Select	ENSP00000260408.3:p.Arg142ThrfsTer?
ENST00000260408.7:c.424_425insCAGAG	ENSP00000260408.3:p.Arg142ThrfsTer?
ENST00000396136.6:c.99_100insCAGAG
ENST00000402627.5:c.56-38354_56-38353insCAGAG	ENSP00000386056.1:n.56-38354_56-38353insCAGAG
ENST00000439637.5:c.325+3012_325+3013insCAGAG	ENSP00000391930.1:n.325+3012_325+3013insCAGAG
ENST00000497846.5:n.541_542insCAGAG
ENST00000558004.1:c.332-13987_332-13986insCAGAG	ENSP00000452704.1:n.332-13987_332-13986insCAGAG
ENST00000558733.5:n.660_661insCAGAG
ENST00000559053.1:c.56-38354_56-38353insCAGAG	ENSP00000453952.1:n.56-38354_56-38353insCAGAG
ENST00000560608.5:n.562_563insCAGAG
ENST00000561288.1:c.55+70296_55+70297insCAGAG	ENSP00000452639.1:n.55+70296_55+70297insCAGAG
NM_001110.3:c.424_425insCAGAG	NP_001101.1:p.Arg142ThrfsTer?
XM_005254117.2:c.424_425insCAGAG	XP_005254174.1:p.Arg142ThrfsTer?
NM_001320570.1:c.424_425insCAGAG	NP_001307499.1:p.Arg142ThrfsTer?
XM_024449818.1:c.202_203insCAGAG	XP_024305586.1:p.Arg68ThrfsTer?
NM_001110.4:c.424_425insCAGAG MANE Select	NP_001101.1:p.Arg142ThrfsTer?
NM_001320570.2:c.424_425insCAGAG	NP_001307499.1:p.Arg142ThrfsTer?