Canonical Allele Identifier: CA2339606550
Gene: CRX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47834568_47834569delinsAC , CM000681.2:g.47834568_47834569delinsAC GRCh38
NC_000019.9:g.48337825_48337826delinsAC , CM000681.1:g.48337825_48337826delinsAC GRCh37
NC_000019.8:g.53029637_53029638delinsAC NCBI36
NG_008605.1:g.17727_17728delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000221996.12:c.100+25_100+26delinsAC MANE Select ENSP00000221996.5:n.100+25_100+26delinsAC...
ENST00000221996.11:c.100+25_100+26delinsAC ENSP00000221996.5:n.100+25_100+26delinsAC...
ENST00000539067.5:c.100+25_100+26delinsAC ENSP00000445565.1:n.100+25_100+26delinsAC...
ENST00000556527.1:n.78-1675_78-1674delinsAC
ENST00000566686.5:c.100+25_100+26delinsAC ENSP00000457808.2:n.100+25_100+26delinsAC...
ENST00000613299.1:c.100+25_100+26delinsAC ENSP00000478106.1:n.100+25_100+26delinsAC...
NM_000554.4:c.100+25_100+26delinsAC NP_000545.1:n.100+25_100+26delinsAC
NM_000554.5:c.100+25_100+26delinsAC NP_000545.1:n.100+25_100+26delinsAC
NM_000554.6:c.100+25_100+26delinsAC MANE Select NP_000545.1:n.100+25_100+26delinsAC
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