Canonical Allele Identifier: CA618154198

Gene: ADAM10

Linked Data

• dbSNP Id: rs1487737470
• gnomAD v2: 15-59001027-A-G
• gnomAD v3: 15-58708828-A-G
• gnomAD v4: 15-58708828-A-G
• MyVariant Identifiers: chr15:g.59001027A>G (hg19) ; chr15:g.58708828A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58708828A>G , CM000677.2:g.58708828A>G	GRCh38
NC_000015.9:g.59001027A>G , CM000677.1:g.59001027A>G	GRCh37
NC_000015.8:g.56788319A>G	NCBI36
NG_033876.1:g.46151T>C
NG_033876.2:g.45880T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.206+8749T>C MANE Select	ENSP00000260408.3:n.206+8749T>C
ENST00000260408.7:c.206+8749T>C	ENSP00000260408.3:n.206+8749T>C
ENST00000402627.5:c.55+40652T>C	ENSP00000386056.1:n.55+40652T>C
ENST00000439637.5:c.206+8749T>C	ENSP00000391930.1:n.206+8749T>C
ENST00000497846.5:n.323+8749T>C
ENST00000558004.1:c.206+8749T>C	ENSP00000452704.1:n.206+8749T>C
ENST00000558733.5:n.442+8749T>C
ENST00000559053.1:c.55+40652T>C	ENSP00000453952.1:n.55+40652T>C
ENST00000560608.5:n.463+8749T>C
ENST00000561149.1:n.393-1448T>C
ENST00000561288.1:c.55+40652T>C	ENSP00000452639.1:n.55+40652T>C
NM_001110.3:c.206+8749T>C	NP_001101.1:n.206+8749T>C
XM_005254117.2:c.206+8749T>C	XP_005254174.1:n.206+8749T>C
NM_001320570.1:c.206+8749T>C	NP_001307499.1:n.206+8749T>C
XM_024449818.1:c.-17+8749T>C	XP_024305586.1:n.-17+8749T>C
NM_001110.4:c.206+8749T>C MANE Select	NP_001101.1:n.206+8749T>C
NM_001320570.2:c.206+8749T>C	NP_001307499.1:n.206+8749T>C