Canonical Allele Identifier: CA1594211700

Gene: ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157515256_157515257delinsCG , CM000667.2:g.157515256_157515257delinsCG	GRCh38
NC_000005.9:g.156942264_156942265delinsCG , CM000667.1:g.156942264_156942265delinsCG	GRCh37
NC_000005.8:g.156874842_156874843delinsCG	NCBI36
NG_046960.1:g.65567_65568delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.667-1752_667-1751delinsCG MANE Select	ENSP00000257527.5:n.667-1752_667-1751delinsCG
ENST00000257527.8:c.667-1752_667-1751delinsCG	ENSP00000257527.4:n.667-1752_667-1751delinsCG
ENST00000517905.1:c.667-1752_667-1751delinsCG	ENSP00000428654.1:n.667-1752_667-1751delinsCG
ENST00000517951.5:c.667-1752_667-1751delinsCG	ENSP00000428376.1:n.667-1752_667-1751delinsCG
NM_033274.4:c.667-1752_667-1751delinsCG	NP_150377.1:n.667-1752_667-1751delinsCG
XM_005266003.2:c.667-1752_667-1751delinsCG	XP_005266060.1:n.667-1752_667-1751delinsCG
XM_011534680.1:c.-135-1752_-135-1751delinsCG	XP_011532982.1:n.-135-1752_-135-1751delinsCG
XM_011534681.1:c.-145-1752_-145-1751delinsCG	XP_011532983.1:n.-145-1752_-145-1751delinsCG
NM_033274.5:c.667-1752_667-1751delinsCG MANE Select	NP_150377.1:n.667-1752_667-1751delinsCG