Canonical Allele Identifier: CA2317756549
Gene: REEP6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1496220C= , CM000681.2:g.1496220C= GRCh38
NC_000019.9:g.1496219C= , CM000681.1:g.1496219C= GRCh37
NC_000019.8:g.1447219C= NCBI36
NG_055254.1:g.10216C=

Transcript Alleles

HGVS Amino-acid change
ENST00000233596.8:c.349-65C= MANE Select ENSP00000233596.2:n.349-65C=
ENST00000395479.10:c.349-65C= MANE Plus Clinical ENSP00000378861.5:n.349-65C=
ENST00000233596.7:c.349-65C= ENSP00000233596.2:n.349-65C=
ENST00000395479.8:c.165-65C=
ENST00000395484.4:c.133-65C= ENSP00000378865.4:n.133-65C=
NM_138393.1:c.349-65C= NP_612402.1:n.349-65C=
NM_001329556.2:c.349-65C= NP_001316485.1:n.349-65C=
NM_138393.3:c.349-65C= NP_612402.1:n.349-65C=
NM_138393.4:c.349-65C= MANE Select NP_612402.1:n.349-65C=
NM_001329556.3:c.349-65C= MANE Plus Clinical NP_001316485.1:n.349-65C=
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