Canonical Allele Identifier: CA1594218024
Gene: ADAM19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157568861G= , CM000667.2:g.157568861G= GRCh38
NC_000005.9:g.156995869G= , CM000667.1:g.156995869G= GRCh37
NC_000005.8:g.156928447G= NCBI36
NG_046960.1:g.11963C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257527.9:c.180+2034C= MANE Select ENSP00000257527.5:n.180+2034C=
ENST00000257527.8:c.180+2034C= ENSP00000257527.4:n.180+2034C=
ENST00000517905.1:c.180+2034C= ENSP00000428654.1:n.180+2034C=
ENST00000517951.5:c.180+2034C= ENSP00000428376.1:n.180+2034C=
NM_033274.4:c.180+2034C= NP_150377.1:n.180+2034C=
XM_005266003.2:c.180+2034C= XP_005266060.1:n.180+2034C=
NM_033274.5:c.180+2034C= MANE Select NP_150377.1:n.180+2034C=
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