Canonical Allele Identifier: CA1083372856
Gene: ADAM19 HGNC NCBI

Linked Data

gnomAD v3: 5-157518143-C-CAAAAAAA
gnomAD v4: 5-157518143-C-CAAAAAAA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157518147_157518153dup , CM000667.2:g.157518147_157518153dup GRCh38
NC_000005.9:g.156945155_156945161dup , CM000667.1:g.156945155_156945161dup GRCh37
NC_000005.8:g.156877733_156877739dup NCBI36
NG_046960.1:g.62674_62680dup

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.666+673_666+679dup MANE Select ENSP00000257527.5:n.666+673_666+679dup
ENST00000257527.8:c.666+673_666+679dup ENSP00000257527.4:n.666+673_666+679dup
ENST00000517905.1:c.666+673_666+679dup ENSP00000428654.1:n.666+673_666+679dup
ENST00000517951.5:c.666+673_666+679dup ENSP00000428376.1:n.666+673_666+679dup
NM_033274.4:c.666+673_666+679dup NP_150377.1:n.666+673_666+679dup
XM_005266003.2:c.666+673_666+679dup XP_005266060.1:n.666+673_666+679dup
XM_011534680.1:c.-135-4645_-135-4639dup XP_011532982.1:n.-135-4645_-135-4639dup
XM_011534681.1:c.-145-4645_-145-4639dup XP_011532983.1:n.-145-4645_-145-4639dup
NM_033274.5:c.666+673_666+679dup MANE Select NP_150377.1:n.666+673_666+679dup
Search 100 bp 5'
Search 100 bp 3'