Canonical Allele Identifier: CA714356554

Gene: ADAM10

Linked Data

• dbSNP Id: rs1438100203
• gnomAD v3: 15-58741849-G-GT
• gnomAD v4: 15-58741849-G-GT
• MyVariant Identifiers: chr15:g.59034048_59034049insT (hg19) ; chr15:g.58741849_58741850insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58741851dup , CM000677.2:g.58741851dup	GRCh38
NC_000015.9:g.59034050dup , CM000677.1:g.59034050dup	GRCh37
NC_000015.8:g.56821342dup	NCBI36
NG_033876.1:g.13129dup
NG_033876.2:g.12858dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.55+7630dup MANE Select	ENSP00000260408.3:n.55+7630dup
ENST00000260408.7:c.55+7630dup	ENSP00000260408.3:n.55+7630dup
ENST00000402627.5:c.55+7630dup	ENSP00000386056.1:n.55+7630dup
ENST00000439637.5:c.55+7630dup	ENSP00000391930.1:n.55+7630dup
ENST00000497846.5:n.172+6945dup
ENST00000558004.1:c.55+7630dup	ENSP00000452704.1:n.55+7630dup
ENST00000558733.5:n.291+7630dup
ENST00000559053.1:c.55+7630dup	ENSP00000453952.1:n.55+7630dup
ENST00000560608.5:n.312+7630dup
ENST00000561149.1:n.241+7630dup
ENST00000561288.1:c.55+7630dup	ENSP00000452639.1:n.55+7630dup
NM_001110.3:c.55+7630dup	NP_001101.1:n.55+7630dup
XM_005254117.2:c.55+7630dup	XP_005254174.1:n.55+7630dup
NM_001320570.1:c.55+7630dup	NP_001307499.1:n.55+7630dup
XM_024449818.1:c.-168+6945dup	XP_024305586.1:n.-168+6945dup
NM_001110.4:c.55+7630dup MANE Select	NP_001101.1:n.55+7630dup
NM_001320570.2:c.55+7630dup	NP_001307499.1:n.55+7630dup