Canonical Allele Identifier: CA1311552
Community Standard Title: NM_201253.3(CRB1):c.40C>T (p.Leu14Phe)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197268452C>T , CM000663.2:g.197268452C>T GRCh38
NC_000001.10:g.197237582C>T , CM000663.1:g.197237582C>T GRCh37
NC_000001.9:g.195504205C>T NCBI36
NG_008483.1:g.5175C>T
NG_008483.2:g.71991C>T

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.40C>T MANE Select NP_957705.1:p.Leu14Phe
ENST00000367400.8:c.40C>T MANE Select ENSP00000356370.3:p.Leu14Phe
NM_001193640.1:c.40C>T NP_001180569.1:p.Leu14Phe
NM_001193640.2:c.40C>T NP_001180569.1:p.Leu14Phe
NM_001257965.1:c.-212-33988C>T NP_001244894.1:n.-212-33988C>T
NM_001257965.2:c.-212-33988C>T NP_001244894.1:n.-212-33988C>T
NM_001257966.1:c.40C>T NP_001244895.1:p.Leu14Phe
NM_001257966.2:c.40C>T NP_001244895.1:p.Leu14Phe
NM_201253.2:c.40C>T NP_957705.1:p.Leu14Phe
NR_047563.1:n.249C>T
NR_047563.2:n.201C>T
NR_047564.1:n.249C>T
NR_047564.2:n.201C>T
ENST00000367399.6:c.40C>T ENSP00000356369.2:p.Leu14Phe
ENST00000367400.7:c.40C>T ENSP00000356370.3:p.Leu14Phe
ENST00000475659.1:n.177C>T
ENST00000484075.5:c.40C>T ENSP00000433932.1:p.Leu14Phe
ENST00000535699.5:c.-168C>T ENSP00000438786.1:n.-168C>T
ENST00000538660.5:c.40C>T ENSP00000438091.1:p.Leu14Phe
ENST00000638467.1:c.40C>T ENSP00000491102.1:p.Leu14Phe
XM_011509365.1:c.40C>T XP_011507667.1:p.Leu14Phe
XM_011509365.2:c.40C>T XP_011507667.1:p.Leu14Phe
XM_011509366.1:c.40C>T XP_011507668.1:p.Leu14Phe
XM_011509367.1:c.40C>T XP_011507669.1:p.Leu14Phe
XM_011509368.1:c.40C>T XP_011507670.1:p.Leu14Phe
XM_017000851.1:c.-664C>T XP_016856340.1:n.-664C>T
XM_017000852.1:c.40C>T XP_016856341.1:p.Leu14Phe