Canonical Allele Identifier: CA1594211640
Gene: ADAM19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157515099T= , CM000667.2:g.157515099T= GRCh38
NC_000005.9:g.156942107T= , CM000667.1:g.156942107T= GRCh37
NC_000005.8:g.156874685T= NCBI36
NG_046960.1:g.65725A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257527.9:c.667-1594A= MANE Select ENSP00000257527.5:n.667-1594A=
ENST00000257527.8:c.667-1594A= ENSP00000257527.4:n.667-1594A=
ENST00000517905.1:c.667-1594A= ENSP00000428654.1:n.667-1594A=
ENST00000517951.5:c.667-1594A= ENSP00000428376.1:n.667-1594A=
NM_033274.4:c.667-1594A= NP_150377.1:n.667-1594A=
XM_005266003.2:c.667-1594A= XP_005266060.1:n.667-1594A=
XM_011534680.1:c.-135-1594A= XP_011532982.1:n.-135-1594A=
XM_011534681.1:c.-145-1594A= XP_011532983.1:n.-145-1594A=
NM_033274.5:c.667-1594A= MANE Select NP_150377.1:n.667-1594A=