Canonical Allele Identifier: CA1594218582

Gene: ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157543102_157543103delinsCA , CM000667.2:g.157543102_157543103delinsCA	GRCh38
NC_000005.9:g.156970110_156970111delinsCA , CM000667.1:g.156970110_156970111delinsCA	GRCh37
NC_000005.8:g.156902688_156902689delinsCA	NCBI36
NG_046960.1:g.37721_37722delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.252-5112_252-5111delinsTG MANE Select	ENSP00000257527.5:n.252-5112_252-5111delinsTG
ENST00000257527.8:c.252-5112_252-5111delinsTG	ENSP00000257527.4:n.252-5112_252-5111delinsTG
ENST00000517905.1:c.252-5112_252-5111delinsTG	ENSP00000428654.1:n.252-5112_252-5111delinsTG
ENST00000517951.5:c.252-5112_252-5111delinsTG	ENSP00000428376.1:n.252-5112_252-5111delinsTG
NM_033274.4:c.252-5112_252-5111delinsTG	NP_150377.1:n.252-5112_252-5111delinsTG
XM_005266003.2:c.252-5112_252-5111delinsTG	XP_005266060.1:n.252-5112_252-5111delinsTG
NM_033274.5:c.252-5112_252-5111delinsTG MANE Select	NP_150377.1:n.252-5112_252-5111delinsTG