Canonical Allele Identifier: CA2259506314
Gene: RARA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40332945_40332947delinsTAG , CM000679.2:g.40332945_40332947delinsTAG GRCh38
NC_000017.10:g.38489197_38489199delinsTAG , CM000679.1:g.38489197_38489199delinsTAG GRCh37
NC_000017.9:g.35742723_35742725delinsTAG NCBI36
NG_027701.1:g.28775_28777delinsTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000254066.10:c.178+1549_178+1551delinsTAG MANE Select ENSP00000254066.5:n.178+1549_178+1551delinsTAG
ENST00000254066.9:c.178+1549_178+1551delinsTAG ENSP00000254066.5:n.178+1549_178+1551delinsTAG
ENST00000394089.6:c.178+1549_178+1551delinsTAG ENSP00000377649.2:n.178+1549_178+1551delinsTAG
ENST00000425707.7:c.178+1549_178+1551delinsTAG ENSP00000389993.3:n.178+1549_178+1551delinsTAG
ENST00000577646.5:c.178+1549_178+1551delinsTAG ENSP00000464287.1:n.178+1549_178+1551delinsTAG
NM_000964.3:c.178+1549_178+1551delinsTAG NP_000955.1:n.178+1549_178+1551delinsTAG
NM_001145301.2:c.178+1549_178+1551delinsTAG NP_001138773.1:n.178+1549_178+1551delinsTAG
NM_001145302.2:c.178+1549_178+1551delinsTAG NP_001138774.1:n.178+1549_178+1551delinsTAG
XM_005257553.1:c.178+1549_178+1551delinsTAG XP_005257610.1:n.178+1549_178+1551delinsTAG
XM_005257554.1:c.178+1549_178+1551delinsTAG XP_005257611.1:n.178+1549_178+1551delinsTAG
XM_011525095.1:c.178+1549_178+1551delinsTAG XP_011523397.1:n.178+1549_178+1551delinsTAG
NM_000964.4:c.178+1549_178+1551delinsTAG MANE Select NP_000955.1:n.178+1549_178+1551delinsTAG
NM_001145301.3:c.178+1549_178+1551delinsTAG NP_001138773.1:n.178+1549_178+1551delinsTAG
NM_001145302.3:c.178+1549_178+1551delinsTAG NP_001138774.1:n.178+1549_178+1551delinsTAG