Canonical Allele Identifier: CA1594207259

Gene: ADAM19

Linked Data

• dbSNP Id: rs762312138

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157505446_157505447del , CM000667.2:g.157505446_157505447del	GRCh38
NC_000005.9:g.156932454_156932455del , CM000667.1:g.156932454_156932455del	GRCh37
NC_000005.8:g.156865032_156865033del	NCBI36
NG_046960.1:g.75378_75379del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.1130+223_1130+224del MANE Select	ENSP00000257527.5:n.1130+223_1130+224del
ENST00000257527.8:c.1130+223_1130+224del	ENSP00000257527.4:n.1130+223_1130+224del
ENST00000517905.1:c.1130+223_1130+224del	ENSP00000428654.1:n.1130+223_1130+224del
ENST00000517951.5:c.*321+223_*321+224del	ENSP00000428376.1:n.*321+223_*321+224del
NM_033274.4:c.1130+223_1130+224del	NP_150377.1:n.1130+223_1130+224del
XM_005266003.2:c.1130+223_1130+224del	XP_005266060.1:n.1130+223_1130+224del
XM_011534680.1:c.329+223_329+224del	XP_011532982.1:n.329+223_329+224del
XM_011534681.1:c.329+223_329+224del	XP_011532983.1:n.329+223_329+224del
XM_011534682.1:c.329+223_329+224del	XP_011532984.1:n.329+223_329+224del
XM_011534682.2:c.329+223_329+224del	XP_011532984.1:n.329+223_329+224del
XM_017010009.1:c.329+223_329+224del	XP_016865498.1:n.329+223_329+224del
NM_033274.5:c.1130+223_1130+224del MANE Select	NP_150377.1:n.1130+223_1130+224del