Canonical Allele Identifier: CA392621814

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58957346A>C (hg19) ; chr15:g.58665147A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665147A>C , CM000677.2:g.58665147A>C	GRCh38
NC_000015.9:g.58957346A>C , CM000677.1:g.58957346A>C	GRCh37
NC_000015.8:g.56744638A>C	NCBI36
NG_033876.1:g.89832T>G
NG_033876.2:g.89561T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.535T>G MANE Select	ENSP00000260408.3:p.Phe179Val
ENST00000260408.7:c.535T>G	ENSP00000260408.3:p.Phe179Val
ENST00000396136.6:c.361T>G
ENST00000402627.5:c.56-24317T>G	ENSP00000386056.1:n.56-24317T>G
ENST00000439637.5:c.376T>G
ENST00000558733.5:n.771T>G
ENST00000559053.1:c.56-24317T>G	ENSP00000453952.1:n.56-24317T>G
ENST00000561288.1:c.56-67629T>G	ENSP00000452639.1:n.56-67629T>G
NM_001110.3:c.535T>G	NP_001101.1:p.Phe179Val
XM_005254117.2:c.535T>G	XP_005254174.1:p.Phe179Val
NM_001320570.1:c.535T>G	NP_001307499.1:p.Phe179Val
XM_024449818.1:c.313T>G	XP_024305586.1:p.Phe105Val
NM_001110.4:c.535T>G MANE Select	NP_001101.1:p.Phe179Val
NM_001320570.2:c.535T>G	NP_001307499.1:p.Phe179Val