Canonical Allele Identifier: CA1594212932

Gene: ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157518221C= , CM000667.2:g.157518221C=	GRCh38
NC_000005.9:g.156945229C= , CM000667.1:g.156945229C=	GRCh37
NC_000005.8:g.156877807C=	NCBI36
NG_046960.1:g.62603G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.666+602G= MANE Select	ENSP00000257527.5:n.666+602G=
ENST00000257527.8:c.666+602G=	ENSP00000257527.4:n.666+602G=
ENST00000517905.1:c.666+602G=	ENSP00000428654.1:n.666+602G=
ENST00000517951.5:c.666+602G=	ENSP00000428376.1:n.666+602G=
NM_033274.4:c.666+602G=	NP_150377.1:n.666+602G=
XM_005266003.2:c.666+602G=	XP_005266060.1:n.666+602G=
XM_011534680.1:c.-135-4716G=	XP_011532982.1:n.-135-4716G=
XM_011534681.1:c.-145-4716G=	XP_011532983.1:n.-145-4716G=
NM_033274.5:c.666+602G= MANE Select	NP_150377.1:n.666+602G=