Canonical Allele Identifier: CA2259506268

Gene: RARA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40332819_40332820delinsAG , CM000679.2:g.40332819_40332820delinsAG	GRCh38
NC_000017.10:g.38489071_38489072delinsAG , CM000679.1:g.38489071_38489072delinsAG	GRCh37
NC_000017.9:g.35742597_35742598delinsAG	NCBI36
NG_027701.1:g.28649_28650delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.178+1423_178+1424delinsAG MANE Select	ENSP00000254066.5:n.178+1423_178+1424delinsAG
ENST00000254066.9:c.178+1423_178+1424delinsAG	ENSP00000254066.5:n.178+1423_178+1424delinsAG
ENST00000394089.6:c.178+1423_178+1424delinsAG	ENSP00000377649.2:n.178+1423_178+1424delinsAG
ENST00000425707.7:c.178+1423_178+1424delinsAG	ENSP00000389993.3:n.178+1423_178+1424delinsAG
ENST00000577646.5:c.178+1423_178+1424delinsAG	ENSP00000464287.1:n.178+1423_178+1424delinsAG
NM_000964.3:c.178+1423_178+1424delinsAG	NP_000955.1:n.178+1423_178+1424delinsAG
NM_001145301.2:c.178+1423_178+1424delinsAG	NP_001138773.1:n.178+1423_178+1424delinsAG
NM_001145302.2:c.178+1423_178+1424delinsAG	NP_001138774.1:n.178+1423_178+1424delinsAG
XM_005257553.1:c.178+1423_178+1424delinsAG	XP_005257610.1:n.178+1423_178+1424delinsAG
XM_005257554.1:c.178+1423_178+1424delinsAG	XP_005257611.1:n.178+1423_178+1424delinsAG
XM_011525095.1:c.178+1423_178+1424delinsAG	XP_011523397.1:n.178+1423_178+1424delinsAG
NM_000964.4:c.178+1423_178+1424delinsAG MANE Select	NP_000955.1:n.178+1423_178+1424delinsAG
NM_001145301.3:c.178+1423_178+1424delinsAG	NP_001138773.1:n.178+1423_178+1424delinsAG
NM_001145302.3:c.178+1423_178+1424delinsAG	NP_001138774.1:n.178+1423_178+1424delinsAG