Canonical Allele Identifier: CA130179778

Gene: ADAM19

Linked Data

• dbSNP Id: rs762312138
• MyVariant Identifiers: chr5:g.156932452_156932453insA (hg19) ; chr5:g.157505444_157505445insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157505447dup , CM000667.2:g.157505447dup	GRCh38
NC_000005.9:g.156932455dup , CM000667.1:g.156932455dup	GRCh37
NC_000005.8:g.156865033dup	NCBI36
NG_046960.1:g.75379dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.1130+224dup MANE Select	ENSP00000257527.5:n.1130+224dup
ENST00000257527.8:c.1130+224dup	ENSP00000257527.4:n.1130+224dup
ENST00000517905.1:c.1130+224dup	ENSP00000428654.1:n.1130+224dup
ENST00000517951.5:c.*321+224dup	ENSP00000428376.1:n.*321+224dup
NM_033274.4:c.1130+224dup	NP_150377.1:n.1130+224dup
XM_005266003.2:c.1130+224dup	XP_005266060.1:n.1130+224dup
XM_011534680.1:c.329+224dup	XP_011532982.1:n.329+224dup
XM_011534681.1:c.329+224dup	XP_011532983.1:n.329+224dup
XM_011534682.1:c.329+224dup	XP_011532984.1:n.329+224dup
XM_011534682.2:c.329+224dup	XP_011532984.1:n.329+224dup
XM_017010009.1:c.329+224dup	XP_016865498.1:n.329+224dup
NM_033274.5:c.1130+224dup MANE Select	NP_150377.1:n.1130+224dup