Canonical Allele Identifier: CA1594186808

Gene: ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157489581A= , CM000667.2:g.157489581A=	GRCh38
NC_000005.9:g.156916589A= , CM000667.1:g.156916589A=	GRCh37
NC_000005.8:g.156849167A=	NCBI36
NG_046960.1:g.91243T=

Transcript Alleles

HGVS	Amino-acid Change
NM_033274.5:c.2241-395T= MANE Select	NP_150377.1:n.2241-395T=
ENST00000257527.9:c.2241-395T= MANE Select	ENSP00000257527.5:n.2241-395T=
NM_033274.4:c.2241-395T=	NP_150377.1:n.2241-395T=
ENST00000257527.8:c.2241-395T=	ENSP00000257527.4:n.2241-395T=
ENST00000517374.5:c.953-395T=
ENST00000517905.1:c.2241-395T=	ENSP00000428654.1:n.2241-395T=
ENST00000517951.5:c.*1432-395T=	ENSP00000428376.1:n.*1432-395T=
XM_005266003.2:c.2241-395T=	XP_005266060.1:n.2241-395T=
XM_011534680.1:c.1440-395T=	XP_011532982.1:n.1440-395T=
XM_011534681.1:c.1440-395T=	XP_011532983.1:n.1440-395T=
XM_011534682.1:c.1440-395T=	XP_011532984.1:n.1440-395T=
XM_011534682.2:c.1440-395T=	XP_011532984.1:n.1440-395T=
XM_017010009.1:c.1440-395T=	XP_016865498.1:n.1440-395T=