Canonical Allele Identifier: CA806248995

Gene: ADAM19

Linked Data

• dbSNP Id: rs1160903688
• MyVariant Identifiers: chr5:g.156970196del (hg19) ; chr5:g.157543188del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157543188del , CM000667.2:g.157543188del	GRCh38
NC_000005.9:g.156970196del , CM000667.1:g.156970196del	GRCh37
NC_000005.8:g.156902774del	NCBI36
NG_046960.1:g.37636del

Transcript Alleles

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