Canonical Allele Identifier: CA175839965

Gene: ADAM18

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.39690859C>A , CM000670.2:g.39690859C>A	GRCh38
NC_000008.10:g.39548378C>A , CM000670.1:g.39548378C>A	GRCh37
NC_000008.9:g.39667535C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265707.10:c.1822-1741C>A MANE Select	ENSP00000265707.5:n.1822-1741C>A
ENST00000265707.9:c.1822-1741C>A	ENSP00000265707.5:n.1822-1741C>A
ENST00000379866.5:c.1750-1741C>A	ENSP00000369195.1:n.1750-1741C>A
ENST00000520087.5:c.1460-1741C>A	ENSP00000428083.1:n.1460-1741C>A
ENST00000523755.5:n.284-1741C>A
ENST00000524117.1:n.240-1741C>A
NM_014237.2:c.1822-1741C>A	NP_055052.1:n.1822-1741C>A
XR_247133.2:n.1581-1741C>A
NM_001320313.1:c.1750-1741C>A	NP_001307242.1:n.1750-1741C>A
NR_135201.1:n.1515-1741C>A
NM_014237.3:c.1822-1741C>A MANE Select	NP_055052.1:n.1822-1741C>A
NM_001320313.2:c.1750-1741C>A	NP_001307242.1:n.1750-1741C>A
NR_135201.2:n.1515-1741C>A