Canonical Allele Identifier: CA2628685383

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58610801-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610801A>G , CM000677.2:g.58610801A>G	GRCh38
NC_000015.9:g.58903000A>G , CM000677.1:g.58903000A>G	GRCh37
NC_000015.8:g.56690292A>G	NCBI36
NG_033876.1:g.144178T>C
NG_033876.2:g.143907T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1804+198T>C MANE Select	ENSP00000260408.3:n.1804+198T>C
ENST00000260408.7:c.1804+198T>C	ENSP00000260408.3:n.1804+198T>C
ENST00000396136.6:c.1630+198T>C
ENST00000402627.5:c.155-13283T>C	ENSP00000386056.1:n.155-13283T>C
ENST00000470269.5:n.333+198T>C
ENST00000482945.5:n.1225T>C
ENST00000561288.1:c.56-13283T>C	ENSP00000452639.1:n.56-13283T>C
NM_001110.3:c.1804+198T>C	NP_001101.1:n.1804+198T>C
XM_005254117.2:c.1711+198T>C	XP_005254174.1:n.1711+198T>C
NM_001320570.1:c.1711+198T>C	NP_001307499.1:n.1711+198T>C
XM_024449818.1:c.1582+198T>C	XP_024305586.1:n.1582+198T>C
NM_001110.4:c.1804+198T>C MANE Select	NP_001101.1:n.1804+198T>C
NM_001320570.2:c.1711+198T>C	NP_001307499.1:n.1711+198T>C