Canonical Allele Identifier: CA15838251
Gene: ADAM10 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2305421

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58610884A>G , CM000677.2:g.58610884A>G GRCh38
NC_000015.9:g.58903083A>G , CM000677.1:g.58903083A>G GRCh37
NC_000015.8:g.56690375A>G NCBI36
NG_033876.1:g.144095T>C

Transcript Alleles

HGVS Amino-acid change
NM_001110.3:c.1804+115T>C VV NP_001101.1:p.=
XM_005254117.2:c.1711+115T>C XP_005254174.1:p.=
NM_001320570.1:c.1711+115T>C VV NP_001307499.1:p.=
XM_024449818.1:c.1582+115T>C XP_024305586.1:p.=
NM_001110.4:c.1804+115T>C VV MANE Preferred NP_001101.1:p.=
ENST00000260408.7:c.1804+115T>C ENSP00000260408.3:p.=
ENST00000396136.6:n.1630+115T>C
ENST00000402627.5:c.155-13366T>C ENSP00000386056.1:p.=
ENST00000470269.5:n.333+115T>C
ENST00000482945.5:n.1142T>C
ENST00000561288.1:c.56-13366T>C ENSP00000452639.1:p.=