Canonical Allele Identifier: CA1594212892
Gene: ADAM19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157518143_157518144delinsCA , CM000667.2:g.157518143_157518144delinsCA GRCh38
NC_000005.9:g.156945151_156945152delinsCA , CM000667.1:g.156945151_156945152delinsCA GRCh37
NC_000005.8:g.156877729_156877730delinsCA NCBI36
NG_046960.1:g.62680_62681delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.666+679_666+680delinsTG MANE Select ENSP00000257527.5:n.666+679_666+680delins...
ENST00000257527.8:c.666+679_666+680delinsTG ENSP00000257527.4:n.666+679_666+680delins...
ENST00000517905.1:c.666+679_666+680delinsTG ENSP00000428654.1:n.666+679_666+680delins...
ENST00000517951.5:c.666+679_666+680delinsTG ENSP00000428376.1:n.666+679_666+680delins...
NM_033274.4:c.666+679_666+680delinsTG NP_150377.1:n.666+679_666+680delinsTG
XM_005266003.2:c.666+679_666+680delinsTG XP_005266060.1:n.666+679_666+680delinsTG
XM_011534680.1:c.-135-4639_-135-4638delinsTG XP_011532982.1:n.-135-4639_-135-4638delin...
XM_011534681.1:c.-145-4639_-145-4638delinsTG XP_011532983.1:n.-145-4639_-145-4638delin...
NM_033274.5:c.666+679_666+680delinsTG MANE Select NP_150377.1:n.666+679_666+680delinsTG