Canonical Allele Identifier: CA1883176858

Gene: RXRA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408353_134408354delinsCA , CM000671.2:g.134408353_134408354delinsCA	GRCh38
NC_000009.11:g.137300199_137300200delinsCA , CM000671.1:g.137300199_137300200delinsCA	GRCh37
NC_000009.10:g.136440020_136440021delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.430+54_430+55delinsCA MANE Select	ENSP00000419692.1:n.430+54_430+55delinsCA
ENST00000672570.1:c.349+54_349+55delinsCA	ENSP00000500402.1:n.349+54_349+55delinsCA
ENST00000356384.4:n.840+54_840+55delinsCA
ENST00000481739.1:c.430+54_430+55delinsCA	ENSP00000419692.1:n.430+54_430+55delinsCA
NM_001291920.1:c.349+54_349+55delinsCA	NP_001278849.1:n.349+54_349+55delinsCA
NM_001291921.1:c.139+54_139+55delinsCA	NP_001278850.1:n.139+54_139+55delinsCA
NM_002957.5:c.430+54_430+55delinsCA	NP_002948.1:n.430+54_430+55delinsCA
NM_002957.6:c.430+54_430+55delinsCA MANE Select	NP_002948.1:n.430+54_430+55delinsCA
NM_001291921.2:c.139+54_139+55delinsCA	NP_001278850.1:n.139+54_139+55delinsCA
NM_001291920.2:c.349+54_349+55delinsCA	NP_001278849.1:n.349+54_349+55delinsCA