Canonical Allele Identifier: CA2180485107

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58741904_58741907delinsCCTT , CM000677.2:g.58741904_58741907delinsCCTT	GRCh38
NC_000015.9:g.59034103_59034106delinsCCTT , CM000677.1:g.59034103_59034106delinsCCTT	GRCh37
NC_000015.8:g.56821395_56821398delinsCCTT	NCBI36
NG_033876.1:g.13072_13075delinsAAGG
NG_033876.2:g.12801_12804delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.55+7573_55+7576delinsAAGG MANE Select	ENSP00000260408.3:n.55+7573_55+7576delinsAAGG
ENST00000260408.7:c.55+7573_55+7576delinsAAGG	ENSP00000260408.3:n.55+7573_55+7576delinsAAGG
ENST00000402627.5:c.55+7573_55+7576delinsAAGG	ENSP00000386056.1:n.55+7573_55+7576delinsAAGG
ENST00000439637.5:c.55+7573_55+7576delinsAAGG	ENSP00000391930.1:n.55+7573_55+7576delinsAAGG
ENST00000497846.5:n.172+6888_172+6891delinsAAGG
ENST00000558004.1:c.55+7573_55+7576delinsAAGG	ENSP00000452704.1:n.55+7573_55+7576delinsAAGG
ENST00000558733.5:n.291+7573_291+7576delinsAAGG
ENST00000559053.1:c.55+7573_55+7576delinsAAGG	ENSP00000453952.1:n.55+7573_55+7576delinsAAGG
ENST00000560608.5:n.312+7573_312+7576delinsAAGG
ENST00000561149.1:n.241+7573_241+7576delinsAAGG
ENST00000561288.1:c.55+7573_55+7576delinsAAGG	ENSP00000452639.1:n.55+7573_55+7576delinsAAGG
NM_001110.3:c.55+7573_55+7576delinsAAGG	NP_001101.1:n.55+7573_55+7576delinsAAGG
XM_005254117.2:c.55+7573_55+7576delinsAAGG	XP_005254174.1:n.55+7573_55+7576delinsAAGG
NM_001320570.1:c.55+7573_55+7576delinsAAGG	NP_001307499.1:n.55+7573_55+7576delinsAAGG
XM_024449818.1:c.-168+6888_-168+6891delinsAAGG	XP_024305586.1:n.-168+6888_-168+6891delinsAAGG
NM_001110.4:c.55+7573_55+7576delinsAAGG MANE Select	NP_001101.1:n.55+7573_55+7576delinsAAGG
NM_001320570.2:c.55+7573_55+7576delinsAAGG	NP_001307499.1:n.55+7573_55+7576delinsAAGG