Canonical Allele Identifier: CA1188974209
Gene: RAP1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111564994C= , CM000663.2:g.111564994C= GRCh38
NC_000001.10:g.112107616C= , CM000663.1:g.112107616C= GRCh37
NC_000001.9:g.111909139C= NCBI36
NG_032119.1:g.3982G= , LRG_424:g.3982G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356415.5:c.-28+22485C= ENSP00000348786.1:n.-28+22485C=
XM_017001964.1:c.-28+22485C= XP_016857453.1:n.-28+22485C=
NM_001370216.1:c.-28+22485C= NP_001357145.1:n.-28+22485C=
NM_001370216.2:c.-28+22485C= NP_001357145.1:n.-28+22485C=