Canonical Allele Identifier: CA1594207143
Gene: ADAM19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157505326G= , CM000667.2:g.157505326G= GRCh38
NC_000005.9:g.156932334G= , CM000667.1:g.156932334G= GRCh37
NC_000005.8:g.156864912G= NCBI36
NG_046960.1:g.75498C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257527.9:c.1130+343C= MANE Select ENSP00000257527.5:n.1130+343C=
ENST00000257527.8:c.1130+343C= ENSP00000257527.4:n.1130+343C=
ENST00000517905.1:c.1130+343C= ENSP00000428654.1:n.1130+343C=
ENST00000517951.5:c.*321+343C= ENSP00000428376.1:n.*321+343C=
NM_033274.4:c.1130+343C= NP_150377.1:n.1130+343C=
XM_005266003.2:c.1130+343C= XP_005266060.1:n.1130+343C=
XM_011534680.1:c.329+343C= XP_011532982.1:n.329+343C=
XM_011534681.1:c.329+343C= XP_011532983.1:n.329+343C=
XM_011534682.1:c.329+343C= XP_011532984.1:n.329+343C=
XM_011534682.2:c.329+343C= XP_011532984.1:n.329+343C=
XM_017010009.1:c.329+343C= XP_016865498.1:n.329+343C=
NM_033274.5:c.1130+343C= MANE Select NP_150377.1:n.1130+343C=