Canonical Allele Identifier: CA1188974168
Gene: RAP1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111564881C= , CM000663.2:g.111564881C= GRCh38
NC_000001.10:g.112107503C= , CM000663.1:g.112107503C= GRCh37
NC_000001.9:g.111909026C= NCBI36
NG_032119.1:g.4095G= , LRG_424:g.4095G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356415.5:c.-28+22372C= ENSP00000348786.1:n.-28+22372C=
XM_017001964.1:c.-28+22372C= XP_016857453.1:n.-28+22372C=
NM_001370216.1:c.-28+22372C= NP_001357145.1:n.-28+22372C=
NM_001370216.2:c.-28+22372C= NP_001357145.1:n.-28+22372C=