Canonical Allele Identifier: CA1594207253

Gene: ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157505444_157505446delinsTAA , CM000667.2:g.157505444_157505446delinsTAA	GRCh38
NC_000005.9:g.156932452_156932454delinsTAA , CM000667.1:g.156932452_156932454delinsTAA	GRCh37
NC_000005.8:g.156865030_156865032delinsTAA	NCBI36
NG_046960.1:g.75378_75380delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.1130+223_1130+225delinsTTA MANE Select	ENSP00000257527.5:n.1130+223_1130+225delinsTTA
ENST00000257527.8:c.1130+223_1130+225delinsTTA	ENSP00000257527.4:n.1130+223_1130+225delinsTTA
ENST00000517905.1:c.1130+223_1130+225delinsTTA	ENSP00000428654.1:n.1130+223_1130+225delinsTTA
ENST00000517951.5:c.*321+223_*321+225delinsTTA	ENSP00000428376.1:n.*321+223_*321+225delinsTTA
NM_033274.4:c.1130+223_1130+225delinsTTA	NP_150377.1:n.1130+223_1130+225delinsTTA
XM_005266003.2:c.1130+223_1130+225delinsTTA	XP_005266060.1:n.1130+223_1130+225delinsTTA
XM_011534680.1:c.329+223_329+225delinsTTA	XP_011532982.1:n.329+223_329+225delinsTTA
XM_011534681.1:c.329+223_329+225delinsTTA	XP_011532983.1:n.329+223_329+225delinsTTA
XM_011534682.1:c.329+223_329+225delinsTTA	XP_011532984.1:n.329+223_329+225delinsTTA
XM_011534682.2:c.329+223_329+225delinsTTA	XP_011532984.1:n.329+223_329+225delinsTTA
XM_017010009.1:c.329+223_329+225delinsTTA	XP_016865498.1:n.329+223_329+225delinsTTA
NM_033274.5:c.1130+223_1130+225delinsTTA MANE Select	NP_150377.1:n.1130+223_1130+225delinsTTA