Canonical Allele Identifier: CA344038603
Community Standard Title: NM_201253.3(CRB1):c.2640T>G (p.Asn880Lys)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197427965T>G , CM000663.2:g.197427965T>G GRCh38
NC_000001.10:g.197397095T>G , CM000663.1:g.197397095T>G GRCh37
NC_000001.9:g.195663718T>G NCBI36
NG_008483.1:g.164688T>G
NG_008483.2:g.231504T>G

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.2640T>G MANE Select NP_957705.1:p.Asn880Lys
ENST00000367400.8:c.2640T>G MANE Select ENSP00000356370.3:p.Asn880Lys
NM_001193640.1:c.2304T>G NP_001180569.1:p.Asn768Lys
NM_001193640.2:c.2304T>G NP_001180569.1:p.Asn768Lys
NM_001257965.1:c.2433T>G NP_001244894.1:p.Asn811Lys
NM_001257965.2:c.2433T>G NP_001244894.1:p.Asn811Lys
NM_001257966.1:c.2128+6009T>G NP_001244895.1:n.2128+6009T>G
NM_001257966.2:c.2128+6009T>G NP_001244895.1:n.2128+6009T>G
NM_201253.2:c.2640T>G NP_957705.1:p.Asn880Lys
NR_047563.1:n.2641T>G
NR_047563.2:n.2593T>G
NR_047564.1:n.2849T>G
NR_047564.2:n.2801T>G
ENST00000367397.1:c.783T>G ENSP00000356367.1:p.Asn261Lys
ENST00000367399.6:c.2304T>G ENSP00000356369.2:p.Asn768Lys
ENST00000367400.7:c.2640T>G ENSP00000356370.3:p.Asn880Lys
ENST00000484075.5:c.2640T>G ENSP00000433932.1:p.Asn880Lys
ENST00000535699.5:c.2433T>G ENSP00000438786.1:p.Asn811Lys
ENST00000538660.5:c.2128+6009T>G ENSP00000438091.1:n.2128+6009T>G
ENST00000638467.1:c.2640T>G ENSP00000491102.1:p.Asn880Lys
ENST00000681519.1:c.1521T>G ENSP00000505267.1:p.Asn507Lys
XM_011509365.1:c.2640T>G XP_011507667.1:p.Asn880Lys
XM_011509365.2:c.2640T>G XP_011507667.1:p.Asn880Lys
XM_011509366.1:c.2640T>G XP_011507668.1:p.Asn880Lys
XM_011509367.1:c.2640T>G XP_011507669.1:p.Asn880Lys
XM_011509368.1:c.2058T>G XP_011507670.1:p.Asn686Lys
XM_011509369.1:c.1083T>G XP_011507671.1:p.Asn361Lys
XM_011509369.2:c.1083T>G XP_011507671.1:p.Asn361Lys
XM_017000851.1:c.1797T>G XP_016856340.1:p.Asn599Lys
XM_017000852.1:c.2640T>G XP_016856341.1:p.Asn880Lys