Canonical Allele Identifier: CA271742612

Gene: ADAM10

Linked Data

• dbSNP Id: rs1040109497
• MyVariant Identifiers: chr15:g.59034012G>A (hg19) ; chr15:g.58741813G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58741813G>A , CM000677.2:g.58741813G>A	GRCh38
NC_000015.9:g.59034012G>A , CM000677.1:g.59034012G>A	GRCh37
NC_000015.8:g.56821304G>A	NCBI36
NG_033876.1:g.13166C>T
NG_033876.2:g.12895C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.55+7667C>T MANE Select	ENSP00000260408.3:n.55+7667C>T
ENST00000260408.7:c.55+7667C>T	ENSP00000260408.3:n.55+7667C>T
ENST00000402627.5:c.55+7667C>T	ENSP00000386056.1:n.55+7667C>T
ENST00000439637.5:c.55+7667C>T	ENSP00000391930.1:n.55+7667C>T
ENST00000497846.5:n.172+6982C>T
ENST00000558004.1:c.55+7667C>T	ENSP00000452704.1:n.55+7667C>T
ENST00000558733.5:n.291+7667C>T
ENST00000559053.1:c.55+7667C>T	ENSP00000453952.1:n.55+7667C>T
ENST00000560608.5:n.312+7667C>T
ENST00000561149.1:n.241+7667C>T
ENST00000561288.1:c.55+7667C>T	ENSP00000452639.1:n.55+7667C>T
NM_001110.3:c.55+7667C>T	NP_001101.1:n.55+7667C>T
XM_005254117.2:c.55+7667C>T	XP_005254174.1:n.55+7667C>T
NM_001320570.1:c.55+7667C>T	NP_001307499.1:n.55+7667C>T
XM_024449818.1:c.-168+6982C>T	XP_024305586.1:n.-168+6982C>T
NM_001110.4:c.55+7667C>T MANE Select	NP_001101.1:n.55+7667C>T
NM_001320570.2:c.55+7667C>T	NP_001307499.1:n.55+7667C>T