Canonical Allele Identifier: CA344038148

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396998T>C (hg19) ; chr1:g.197427868T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427868T>C , CM000663.2:g.197427868T>C	GRCh38
NC_000001.10:g.197396998T>C , CM000663.1:g.197396998T>C	GRCh37
NC_000001.9:g.195663621T>C	NCBI36
NG_008483.1:g.164591T>C
NG_008483.2:g.231407T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2543T>C MANE Select	ENSP00000356370.3:p.Phe848Ser
ENST00000638467.1:c.2543T>C	ENSP00000491102.1:p.Phe848Ser
ENST00000681519.1:c.1424T>C	ENSP00000505267.1:p.Phe475Ser
ENST00000367397.1:c.686T>C	ENSP00000356367.1:p.Phe229Ser
ENST00000367399.6:c.2207T>C	ENSP00000356369.2:p.Phe736Ser
ENST00000367400.7:c.2543T>C	ENSP00000356370.3:p.Phe848Ser
ENST00000484075.5:c.2543T>C	ENSP00000433932.1:p.Phe848Ser
ENST00000535699.5:c.2336T>C	ENSP00000438786.1:p.Phe779Ser
ENST00000538660.5:c.2128+5912T>C	ENSP00000438091.1:n.2128+5912T>C
NM_001193640.1:c.2207T>C	NP_001180569.1:p.Phe736Ser
NM_001257965.1:c.2336T>C	NP_001244894.1:p.Phe779Ser
NM_001257966.1:c.2128+5912T>C	NP_001244895.1:n.2128+5912T>C
NM_201253.2:c.2543T>C	NP_957705.1:p.Phe848Ser
NR_047563.1:n.2544T>C
NR_047564.1:n.2752T>C
XM_011509365.1:c.2543T>C	XP_011507667.1:p.Phe848Ser
XM_011509366.1:c.2543T>C	XP_011507668.1:p.Phe848Ser
XM_011509367.1:c.2543T>C	XP_011507669.1:p.Phe848Ser
XM_011509368.1:c.1961T>C	XP_011507670.1:p.Phe654Ser
XM_011509369.1:c.986T>C	XP_011507671.1:p.Phe329Ser
XM_011509365.2:c.2543T>C	XP_011507667.1:p.Phe848Ser
XM_011509369.2:c.986T>C	XP_011507671.1:p.Phe329Ser
XM_017000851.1:c.1700T>C	XP_016856340.1:p.Phe567Ser
XM_017000852.1:c.2543T>C	XP_016856341.1:p.Phe848Ser
NM_201253.3:c.2543T>C MANE Select	NP_957705.1:p.Phe848Ser
NM_001193640.2:c.2207T>C	NP_001180569.1:p.Phe736Ser
NM_001257965.2:c.2336T>C	NP_001244894.1:p.Phe779Ser
NR_047563.2:n.2496T>C
NR_047564.2:n.2704T>C
NM_001257966.2:c.2128+5912T>C	NP_001244895.1:n.2128+5912T>C