Canonical Allele Identifier: CA1594218542
Gene: ADAM19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157543057C= , CM000667.2:g.157543057C= GRCh38
NC_000005.9:g.156970065C= , CM000667.1:g.156970065C= GRCh37
NC_000005.8:g.156902643C= NCBI36
NG_046960.1:g.37767G=

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.252-5066G= MANE Select ENSP00000257527.5:n.252-5066G=
ENST00000257527.8:c.252-5066G= ENSP00000257527.4:n.252-5066G=
ENST00000517905.1:c.252-5066G= ENSP00000428654.1:n.252-5066G=
ENST00000517951.5:c.252-5066G= ENSP00000428376.1:n.252-5066G=
NM_033274.4:c.252-5066G= NP_150377.1:n.252-5066G=
XM_005266003.2:c.252-5066G= XP_005266060.1:n.252-5066G=
NM_033274.5:c.252-5066G= MANE Select NP_150377.1:n.252-5066G=
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