Canonical Allele Identifier: CA806232477

Gene: ADAM19

Linked Data

• dbSNP Id: rs1440823836
• gnomAD v3: 5-157515369-CA-C
• gnomAD v4: 5-157515369-CA-C
• MyVariant Identifiers: chr5:g.156942378del (hg19) ; chr5:g.157515370del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157515371del , CM000667.2:g.157515371del	GRCh38
NC_000005.9:g.156942379del , CM000667.1:g.156942379del	GRCh37
NC_000005.8:g.156874957del	NCBI36
NG_046960.1:g.65454del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.667-1865del MANE Select	ENSP00000257527.5:n.667-1865del
ENST00000257527.8:c.667-1865del	ENSP00000257527.4:n.667-1865del
ENST00000517905.1:c.667-1865del	ENSP00000428654.1:n.667-1865del
ENST00000517951.5:c.667-1865del	ENSP00000428376.1:n.667-1865del
NM_033274.4:c.667-1865del	NP_150377.1:n.667-1865del
XM_005266003.2:c.667-1865del	XP_005266060.1:n.667-1865del
XM_011534680.1:c.-135-1865del	XP_011532982.1:n.-135-1865del
XM_011534681.1:c.-145-1865del	XP_011532983.1:n.-145-1865del
NM_033274.5:c.667-1865del MANE Select	NP_150377.1:n.667-1865del