Canonical Allele Identifier: CA2180427159

Gene: ADAM10

Linked Data

• dbSNP Id: rs1895417861

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610815A>G , CM000677.2:g.58610815A>G	GRCh38
NC_000015.9:g.58903014A>G , CM000677.1:g.58903014A>G	GRCh37
NC_000015.8:g.56690306A>G	NCBI36
NG_033876.1:g.144164T>C
NG_033876.2:g.143893T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1804+184T>C MANE Select	ENSP00000260408.3:n.1804+184T>C
ENST00000260408.7:c.1804+184T>C	ENSP00000260408.3:n.1804+184T>C
ENST00000396136.6:c.1630+184T>C
ENST00000402627.5:c.155-13297T>C	ENSP00000386056.1:n.155-13297T>C
ENST00000470269.5:n.333+184T>C
ENST00000482945.5:n.1211T>C
ENST00000561288.1:c.56-13297T>C	ENSP00000452639.1:n.56-13297T>C
NM_001110.3:c.1804+184T>C	NP_001101.1:n.1804+184T>C
XM_005254117.2:c.1711+184T>C	XP_005254174.1:n.1711+184T>C
NM_001320570.1:c.1711+184T>C	NP_001307499.1:n.1711+184T>C
XM_024449818.1:c.1582+184T>C	XP_024305586.1:n.1582+184T>C
NM_001110.4:c.1804+184T>C MANE Select	NP_001101.1:n.1804+184T>C
NM_001320570.2:c.1711+184T>C	NP_001307499.1:n.1711+184T>C