Canonical Allele Identifier: CA885547850

Gene: RAP1A

Linked Data

• dbSNP Id: rs1198303199
• gnomAD v3: 1-111565004-GGGGTCTAT-G
• gnomAD v4: 1-111565004-GGGGTCTAT-G
• MyVariant Identifiers: chr1:g.112107627_112107634del (hg19) ; chr1:g.111565005_111565012del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111565006_111565013del , CM000663.2:g.111565006_111565013del	GRCh38
NC_000001.10:g.112107628_112107635del , CM000663.1:g.112107628_112107635del	GRCh37
NC_000001.9:g.111909151_111909158del	NCBI36
NG_032119.1:g.3964_3971del , LRG_424:g.3964_3971del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356415.5:c.-28+22497_-28+22504del	ENSP00000348786.1:n.-28+22497_-28+22504del
XM_017001964.1:c.-28+22497_-28+22504del	XP_016857453.1:n.-28+22497_-28+22504del
NM_001370216.1:c.-28+22497_-28+22504del	NP_001357145.1:n.-28+22497_-28+22504del
NM_001370216.2:c.-28+22497_-28+22504del	NP_001357145.1:n.-28+22497_-28+22504del