Canonical Allele Identifier: CA1594218678
Gene: ADAM19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157543137_157543139delinsCCG , CM000667.2:g.157543137_157543139delinsCCG GRCh38
NC_000005.9:g.156970145_156970147delinsCCG , CM000667.1:g.156970145_156970147delinsCCG GRCh37
NC_000005.8:g.156902723_156902725delinsCCG NCBI36
NG_046960.1:g.37685_37687delinsCGG

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.252-5148_252-5146delinsCGG MANE Select ENSP00000257527.5:n.252-5148_252-5146deli...
ENST00000257527.8:c.252-5148_252-5146delinsCGG ENSP00000257527.4:n.252-5148_252-5146deli...
ENST00000517905.1:c.252-5148_252-5146delinsCGG ENSP00000428654.1:n.252-5148_252-5146deli...
ENST00000517951.5:c.252-5148_252-5146delinsCGG ENSP00000428376.1:n.252-5148_252-5146deli...
NM_033274.4:c.252-5148_252-5146delinsCGG NP_150377.1:n.252-5148_252-5146delinsCGG
XM_005266003.2:c.252-5148_252-5146delinsCGG XP_005266060.1:n.252-5148_252-5146delinsC...
NM_033274.5:c.252-5148_252-5146delinsCGG MANE Select NP_150377.1:n.252-5148_252-5146delinsCGG
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