Canonical Allele Identifier: CA1594218683
Gene: ADAM19 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157543138C= , CM000667.2:g.157543138C= GRCh38
NC_000005.9:g.156970146C= , CM000667.1:g.156970146C= GRCh37
NC_000005.8:g.156902724C= NCBI36
NG_046960.1:g.37686G=

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.252-5147G= MANE Select ENSP00000257527.5:n.252-5147G=
ENST00000257527.8:c.252-5147G= ENSP00000257527.4:n.252-5147G=
ENST00000517905.1:c.252-5147G= ENSP00000428654.1:n.252-5147G=
ENST00000517951.5:c.252-5147G= ENSP00000428376.1:n.252-5147G=
NM_033274.4:c.252-5147G= NP_150377.1:n.252-5147G=
XM_005266003.2:c.252-5147G= XP_005266060.1:n.252-5147G=
NM_033274.5:c.252-5147G= MANE Select NP_150377.1:n.252-5147G=
Search 100 bp 5'
Search 100 bp 3'