Canonical Allele Identifier: CA370610747

Gene: ADAM7 ADAM7-AS1 ADAM7-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24499305A>T , CM000670.2:g.24499305A>T	GRCh38
NC_000008.10:g.24356818A>T , CM000670.1:g.24356818A>T	GRCh37
NC_000008.9:g.24412708A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000175238.10:c.1912A>T (ADAM7) MANE Select	ENSP00000175238.5:p.Asn638Tyr
ENST00000380789.5:c.1912A>T (ADAM7)	ENSP00000370166.1:p.Asn638Tyr
ENST00000520720.1:c.1228A>T (ADAM7)	ENSP00000430400.1:p.Asn410Tyr
NM_003817.3:c.1912A>T (ADAM7)	NP_003808.2:p.Asn638Tyr
NR_125808.1:n.79+49235T>A (ADAM7-AS1)
NR_125809.1:n.447-7145T>A (ADAM7-AS2)
XM_005273668.2:c.1912A>T (ADAM7)	XP_005273725.1:p.Asn638Tyr
XM_005273669.2:c.1912A>T (ADAM7)	XP_005273726.1:p.Asn638Tyr
XM_005273670.1:c.1912A>T (ADAM7)	XP_005273727.1:p.Asn638Tyr
XM_005273671.2:c.1912A>T (ADAM7)	XP_005273728.1:p.Asn638Tyr
XM_005273672.2:c.1843-873A>T (ADAM7)	XP_005273729.1:n.1843-873A>T
XM_005273673.1:c.1912A>T (ADAM7)	XP_005273730.1:p.Asn638Tyr
XM_017013943.1:c.1912A>T (ADAM7)	XP_016869432.1:p.Asn638Tyr
NM_003817.4:c.1912A>T (ADAM7) MANE Select	NP_003808.2:p.Asn638Tyr