Canonical Allele Identifier: CA1594218132

Gene: ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157568937_157568939delinsGAC , CM000667.2:g.157568937_157568939delinsGAC	GRCh38
NC_000005.9:g.156995945_156995947delinsGAC , CM000667.1:g.156995945_156995947delinsGAC	GRCh37
NC_000005.8:g.156928523_156928525delinsGAC	NCBI36
NG_046960.1:g.11885_11887delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.180+1956_180+1958delinsGTC MANE Select	ENSP00000257527.5:n.180+1956_180+1958delinsGTC
ENST00000257527.8:c.180+1956_180+1958delinsGTC	ENSP00000257527.4:n.180+1956_180+1958delinsGTC
ENST00000517905.1:c.180+1956_180+1958delinsGTC	ENSP00000428654.1:n.180+1956_180+1958delinsGTC
ENST00000517951.5:c.180+1956_180+1958delinsGTC	ENSP00000428376.1:n.180+1956_180+1958delinsGTC
NM_033274.4:c.180+1956_180+1958delinsGTC	NP_150377.1:n.180+1956_180+1958delinsGTC
XM_005266003.2:c.180+1956_180+1958delinsGTC	XP_005266060.1:n.180+1956_180+1958delinsGTC
NM_033274.5:c.180+1956_180+1958delinsGTC MANE Select	NP_150377.1:n.180+1956_180+1958delinsGTC