Canonical Allele Identifier: CA2259497579
Gene: RARA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40313889A= , CM000679.2:g.40313889A= GRCh38
NC_000017.10:g.38470141A= , CM000679.1:g.38470141A= GRCh37
NC_000017.9:g.35723667A= NCBI36
NG_027701.1:g.9719A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254066.10:c.-363+4603A= MANE Select ENSP00000254066.5:n.-363+4603A=
ENST00000254066.9:c.-363+4603A= ENSP00000254066.5:n.-363+4603A=
ENST00000577646.5:c.-440+4603A= ENSP00000464287.1:n.-440+4603A=
NM_000964.3:c.-363+4603A= NP_000955.1:n.-363+4603A=
XM_011525095.1:c.-440+4603A= XP_011523397.1:n.-440+4603A=
NM_000964.4:c.-363+4603A= MANE Select NP_000955.1:n.-363+4603A=
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