Canonical Allele Identifier: CA1188969366

Gene: RAP1A TMIGD3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111553174A>T , CM000663.2:g.111553174A>T	GRCh38
NC_000001.10:g.112095796A>T , CM000663.1:g.112095796A>T	GRCh37
NC_000001.9:g.111897319A>T	NCBI36
NG_032119.1:g.15802T>A , LRG_424:g.15802T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356415.5:c.-28+10665A>T (RAP1A)	ENSP00000348786.1:n.-28+10665A>T
ENST00000369717.8:c.107+10672T>A (TMIGD3)	ENSP00000358731.4:n.107+10672T>A
ENST00000443498.5:c.89+10672T>A (TMIGD3)	ENSP00000398770.1:n.89+10672T>A
NM_001081976.2:c.107+10672T>A (TMIGD3)	NP_001075445.1:n.107+10672T>A
NM_001302680.1:c.107+10672T>A (TMIGD3)	NP_001289609.1:n.107+10672T>A
XM_017001964.1:c.-28+10665A>T (RAP1A)	XP_016857453.1:n.-28+10665A>T
NM_001370216.1:c.-28+10665A>T (RAP1A)	NP_001357145.1:n.-28+10665A>T
NM_001081976.3:c.107+10672T>A (TMIGD3)	NP_001075445.1:n.107+10672T>A
NM_001302680.2:c.107+10672T>A (TMIGD3)	NP_001289609.1:n.107+10672T>A
NM_001370216.2:c.-28+10665A>T (RAP1A)	NP_001357145.1:n.-28+10665A>T