Canonical Allele Identifier: CA1594211718

Gene: ADAM19

Linked Data

• dbSNP Id: rs1756059704

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157515292_157515296dup , CM000667.2:g.157515292_157515296dup	GRCh38
NC_000005.9:g.156942300_156942304dup , CM000667.1:g.156942300_156942304dup	GRCh37
NC_000005.8:g.156874878_156874882dup	NCBI36
NG_046960.1:g.65528_65532dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.667-1791_667-1787dup MANE Select	ENSP00000257527.5:n.667-1791_667-1787dup
ENST00000257527.8:c.667-1791_667-1787dup	ENSP00000257527.4:n.667-1791_667-1787dup
ENST00000517905.1:c.667-1791_667-1787dup	ENSP00000428654.1:n.667-1791_667-1787dup
ENST00000517951.5:c.667-1791_667-1787dup	ENSP00000428376.1:n.667-1791_667-1787dup
NM_033274.4:c.667-1791_667-1787dup	NP_150377.1:n.667-1791_667-1787dup
XM_005266003.2:c.667-1791_667-1787dup	XP_005266060.1:n.667-1791_667-1787dup
XM_011534680.1:c.-135-1791_-135-1787dup	XP_011532982.1:n.-135-1791_-135-1787dup
XM_011534681.1:c.-145-1791_-145-1787dup	XP_011532983.1:n.-145-1791_-145-1787dup
NM_033274.5:c.667-1791_667-1787dup MANE Select	NP_150377.1:n.667-1791_667-1787dup