Canonical Allele Identifier: CA7585696

Gene: ADAM10

Linked Data

• dbSNP Id: rs756392871
• ExAC: 15:58957248 CA / C
• gnomAD v2: 15-58957248-CA-C
• gnomAD v4: 15-58665049-CA-C
• MyVariant Identifiers: chr15:g.58957249del (hg19) ; chr15:g.58665050del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665052del , CM000677.2:g.58665052del	GRCh38
NC_000015.9:g.58957251del , CM000677.1:g.58957251del	GRCh37
NC_000015.8:g.56744543del	NCBI36
NG_033876.1:g.89929del
NG_033876.2:g.89658del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.585+47del MANE Select	ENSP00000260408.3:n.585+47del
ENST00000260408.7:c.585+47del	ENSP00000260408.3:n.585+47del
ENST00000396136.6:c.411+47del
ENST00000402627.5:c.56-24220del	ENSP00000386056.1:n.56-24220del
ENST00000558733.5:n.821+47del
ENST00000559053.1:c.56-24220del	ENSP00000453952.1:n.56-24220del
ENST00000561288.1:c.56-67532del	ENSP00000452639.1:n.56-67532del
NM_001110.3:c.585+47del	NP_001101.1:n.585+47del
XM_005254117.2:c.585+47del	XP_005254174.1:n.585+47del
NM_001320570.1:c.585+47del	NP_001307499.1:n.585+47del
XM_024449818.1:c.363+47del	XP_024305586.1:n.363+47del
NM_001110.4:c.585+47del MANE Select	NP_001101.1:n.585+47del
NM_001320570.2:c.585+47del	NP_001307499.1:n.585+47del