Canonical Allele Identifier: CA1594211681
Gene: ADAM19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157515211A= , CM000667.2:g.157515211A= GRCh38
NC_000005.9:g.156942219A= , CM000667.1:g.156942219A= GRCh37
NC_000005.8:g.156874797A= NCBI36
NG_046960.1:g.65613T=

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.667-1706T= MANE Select ENSP00000257527.5:n.667-1706T=
ENST00000257527.8:c.667-1706T= ENSP00000257527.4:n.667-1706T=
ENST00000517905.1:c.667-1706T= ENSP00000428654.1:n.667-1706T=
ENST00000517951.5:c.667-1706T= ENSP00000428376.1:n.667-1706T=
NM_033274.4:c.667-1706T= NP_150377.1:n.667-1706T=
XM_005266003.2:c.667-1706T= XP_005266060.1:n.667-1706T=
XM_011534680.1:c.-135-1706T= XP_011532982.1:n.-135-1706T=
XM_011534681.1:c.-145-1706T= XP_011532983.1:n.-145-1706T=
NM_033274.5:c.667-1706T= MANE Select NP_150377.1:n.667-1706T=