Canonical Allele Identifier: CA714332527

Gene: ADAM10

Linked Data

• dbSNP Id: rs1168866392
• MyVariant Identifiers: chr15:g.59000947_59000948insTA (hg19) ; chr15:g.58708748_58708749insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58708752_58708753dup , CM000677.2:g.58708752_58708753dup	GRCh38
NC_000015.9:g.59000951_59000952dup , CM000677.1:g.59000951_59000952dup	GRCh37
NC_000015.8:g.56788243_56788244dup	NCBI36
NG_033876.1:g.46229_46230dup
NG_033876.2:g.45958_45959dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.206+8827_206+8828dup MANE Select	ENSP00000260408.3:n.206+8827_206+8828dup
ENST00000260408.7:c.206+8827_206+8828dup	ENSP00000260408.3:n.206+8827_206+8828dup
ENST00000402627.5:c.55+40730_55+40731dup	ENSP00000386056.1:n.55+40730_55+40731dup
ENST00000439637.5:c.206+8827_206+8828dup	ENSP00000391930.1:n.206+8827_206+8828dup
ENST00000497846.5:n.323+8827_323+8828dup
ENST00000558004.1:c.206+8827_206+8828dup	ENSP00000452704.1:n.206+8827_206+8828dup
ENST00000558733.5:n.442+8827_442+8828dup
ENST00000559053.1:c.55+40730_55+40731dup	ENSP00000453952.1:n.55+40730_55+40731dup
ENST00000560608.5:n.463+8827_463+8828dup
ENST00000561149.1:n.393-1370_393-1369dup
ENST00000561288.1:c.55+40730_55+40731dup	ENSP00000452639.1:n.55+40730_55+40731dup
NM_001110.3:c.206+8827_206+8828dup	NP_001101.1:n.206+8827_206+8828dup
XM_005254117.2:c.206+8827_206+8828dup	XP_005254174.1:n.206+8827_206+8828dup
NM_001320570.1:c.206+8827_206+8828dup	NP_001307499.1:n.206+8827_206+8828dup
XM_024449818.1:c.-17+8827_-17+8828dup	XP_024305586.1:n.-17+8827_-17+8828dup
NM_001110.4:c.206+8827_206+8828dup MANE Select	NP_001101.1:n.206+8827_206+8828dup
NM_001320570.2:c.206+8827_206+8828dup	NP_001307499.1:n.206+8827_206+8828dup