Canonical Allele Identifier: CA1311602

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197328616C>T , CM000663.2:g.197328616C>T	GRCh38
NC_000001.10:g.197297746C>T , CM000663.1:g.197297746C>T	GRCh37
NC_000001.9:g.195564369C>T	NCBI36
NG_008483.1:g.65339C>T
NG_008483.2:g.132155C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201253.3:c.265C>T MANE Select	NP_957705.1:p.Pro89Ser
ENST00000367400.8:c.265C>T MANE Select	ENSP00000356370.3:p.Pro89Ser
NM_001193640.1:c.265C>T	NP_001180569.1:p.Pro89Ser
NM_001193640.2:c.265C>T	NP_001180569.1:p.Pro89Ser
NM_001257965.1:c.58C>T	NP_001244894.1:p.Pro20Ser
NM_001257965.2:c.58C>T	NP_001244894.1:p.Pro20Ser
NM_001257966.1:c.265C>T	NP_001244895.1:p.Pro89Ser
NM_001257966.2:c.265C>T	NP_001244895.1:p.Pro89Ser
NM_201253.2:c.265C>T	NP_957705.1:p.Pro89Ser
NR_047563.1:n.474C>T
NR_047563.2:n.426C>T
NR_047564.1:n.474C>T
NR_047564.2:n.426C>T
ENST00000367399.6:c.265C>T	ENSP00000356369.2:p.Pro89Ser
ENST00000367400.7:c.265C>T	ENSP00000356370.3:p.Pro89Ser
ENST00000475659.1:n.402C>T
ENST00000484075.5:c.265C>T	ENSP00000433932.1:p.Pro89Ser
ENST00000535699.5:c.58C>T	ENSP00000438786.1:p.Pro20Ser
ENST00000538660.5:c.265C>T	ENSP00000438091.1:p.Pro89Ser
ENST00000638467.1:c.265C>T	ENSP00000491102.1:p.Pro89Ser
XM_011509365.1:c.265C>T	XP_011507667.1:p.Pro89Ser
XM_011509365.2:c.265C>T	XP_011507667.1:p.Pro89Ser
XM_011509366.1:c.265C>T	XP_011507668.1:p.Pro89Ser
XM_011509367.1:c.265C>T	XP_011507669.1:p.Pro89Ser
XM_011509368.1:c.71-15665C>T	XP_011507670.1:n.71-15665C>T
XM_017000851.1:c.-439C>T	XP_016856340.1:n.-439C>T
XM_017000852.1:c.265C>T	XP_016856341.1:p.Pro89Ser