Canonical Allele Identifier: CA1594211672
Gene: ADAM19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157515190_157515191delinsAC , CM000667.2:g.157515190_157515191delinsAC GRCh38
NC_000005.9:g.156942198_156942199delinsAC , CM000667.1:g.156942198_156942199delinsAC GRCh37
NC_000005.8:g.156874776_156874777delinsAC NCBI36
NG_046960.1:g.65633_65634delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.667-1686_667-1685delinsGT MANE Select ENSP00000257527.5:n.667-1686_667-1685deli...
ENST00000257527.8:c.667-1686_667-1685delinsGT ENSP00000257527.4:n.667-1686_667-1685deli...
ENST00000517905.1:c.667-1686_667-1685delinsGT ENSP00000428654.1:n.667-1686_667-1685deli...
ENST00000517951.5:c.667-1686_667-1685delinsGT ENSP00000428376.1:n.667-1686_667-1685deli...
NM_033274.4:c.667-1686_667-1685delinsGT NP_150377.1:n.667-1686_667-1685delinsGT
XM_005266003.2:c.667-1686_667-1685delinsGT XP_005266060.1:n.667-1686_667-1685delinsG...
XM_011534680.1:c.-135-1686_-135-1685delinsGT XP_011532982.1:n.-135-1686_-135-1685delin...
XM_011534681.1:c.-145-1686_-145-1685delinsGT XP_011532983.1:n.-145-1686_-145-1685delin...
NM_033274.5:c.667-1686_667-1685delinsGT MANE Select NP_150377.1:n.667-1686_667-1685delinsGT