Canonical Allele Identifier: CA1594218734

Gene: ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157543187_157543188delinsTA , CM000667.2:g.157543187_157543188delinsTA	GRCh38
NC_000005.9:g.156970195_156970196delinsTA , CM000667.1:g.156970195_156970196delinsTA	GRCh37
NC_000005.8:g.156902773_156902774delinsTA	NCBI36
NG_046960.1:g.37636_37637delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.252-5197_252-5196delinsTA MANE Select	ENSP00000257527.5:n.252-5197_252-5196delinsTA
ENST00000257527.8:c.252-5197_252-5196delinsTA	ENSP00000257527.4:n.252-5197_252-5196delinsTA
ENST00000517905.1:c.252-5197_252-5196delinsTA	ENSP00000428654.1:n.252-5197_252-5196delinsTA
ENST00000517951.5:c.252-5197_252-5196delinsTA	ENSP00000428376.1:n.252-5197_252-5196delinsTA
NM_033274.4:c.252-5197_252-5196delinsTA	NP_150377.1:n.252-5197_252-5196delinsTA
XM_005266003.2:c.252-5197_252-5196delinsTA	XP_005266060.1:n.252-5197_252-5196delinsTA
NM_033274.5:c.252-5197_252-5196delinsTA MANE Select	NP_150377.1:n.252-5197_252-5196delinsTA