Canonical Allele Identifier: CA714365625

Gene: ADAM10

Linked Data

• dbSNP Id: rs1243672999
• gnomAD v3: 15-58621406-ATT-A
• gnomAD v4: 15-58621406-ATT-A
• MyVariant Identifiers: chr15:g.58913606_58913607del (hg19) ; chr15:g.58621407_58621408del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621408_58621409del , CM000677.2:g.58621408_58621409del	GRCh38
NC_000015.9:g.58913607_58913608del , CM000677.1:g.58913607_58913608del	GRCh37
NC_000015.8:g.56700899_56700900del	NCBI36
NG_033876.1:g.133571_133572del
NG_033876.2:g.133300_133301del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1511+63_1511+64del MANE Select	ENSP00000260408.3:n.1511+63_1511+64del
ENST00000260408.7:c.1511+63_1511+64del	ENSP00000260408.3:n.1511+63_1511+64del
ENST00000396136.6:c.1337+63_1337+64del
ENST00000402627.5:c.154+11907_154+11908del	ENSP00000386056.1:n.154+11907_154+11908de...
ENST00000462061.1:n.71+63_71+64del
ENST00000470269.5:n.40+63_40+64del
ENST00000475898.1:n.536+63_536+64del
ENST00000481164.1:n.34+63_34+64del
ENST00000482945.5:n.34+63_34+64del
ENST00000561288.1:c.56-23890_56-23889del	ENSP00000452639.1:n.56-23890_56-23889del
NM_001110.3:c.1511+63_1511+64del	NP_001101.1:n.1511+63_1511+64del
XM_005254117.2:c.1418+63_1418+64del	XP_005254174.1:n.1418+63_1418+64del
NM_001320570.1:c.1418+63_1418+64del	NP_001307499.1:n.1418+63_1418+64del
XM_024449818.1:c.1289+63_1289+64del	XP_024305586.1:n.1289+63_1289+64del
NM_001110.4:c.1511+63_1511+64del MANE Select	NP_001101.1:n.1511+63_1511+64del
NM_001320570.2:c.1418+63_1418+64del	NP_001307499.1:n.1418+63_1418+64del