Canonical Allele Identifier: CA344045038

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404049A>C (hg19) ; chr1:g.197434919A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434919A>C , CM000663.2:g.197434919A>C	GRCh38
NC_000001.10:g.197404049A>C , CM000663.1:g.197404049A>C	GRCh37
NC_000001.9:g.195670672A>C	NCBI36
NG_008483.1:g.171642A>C
NG_008483.2:g.238458A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3056A>C MANE Select	ENSP00000356370.3:p.Tyr1019Ser
ENST00000638467.1:c.3056A>C	ENSP00000491102.1:p.Tyr1019Ser
ENST00000681519.1:c.1937A>C	ENSP00000505267.1:p.Tyr646Ser
ENST00000367397.1:c.1199A>C	ENSP00000356367.1:p.Tyr400Ser
ENST00000367399.6:c.2720A>C	ENSP00000356369.2:p.Tyr907Ser
ENST00000367400.7:c.3056A>C	ENSP00000356370.3:p.Tyr1019Ser
ENST00000484075.5:c.3056A>C	ENSP00000433932.1:p.Tyr1019Ser
ENST00000535699.5:c.2984A>C	ENSP00000438786.1:p.Tyr995Ser
ENST00000538660.5:c.2129-681A>C	ENSP00000438091.1:n.2129-681A>C
NM_001193640.1:c.2720A>C	NP_001180569.1:p.Tyr907Ser
NM_001257965.1:c.2984A>C	NP_001244894.1:p.Tyr995Ser
NM_001257966.1:c.2129-681A>C	NP_001244895.1:n.2129-681A>C
NM_201253.2:c.3056A>C	NP_957705.1:p.Tyr1019Ser
NR_047563.1:n.3057A>C
NR_047564.1:n.3265A>C
XM_011509365.1:c.3056A>C	XP_011507667.1:p.Tyr1019Ser
XM_011509366.1:c.3056A>C	XP_011507668.1:p.Tyr1019Ser
XM_011509367.1:c.3056A>C	XP_011507669.1:p.Tyr1019Ser
XM_011509368.1:c.2474A>C	XP_011507670.1:p.Tyr825Ser
XM_011509369.1:c.1499A>C	XP_011507671.1:p.Tyr500Ser
XM_011509365.2:c.3056A>C	XP_011507667.1:p.Tyr1019Ser
XM_011509369.2:c.1499A>C	XP_011507671.1:p.Tyr500Ser
XM_017000851.1:c.2213A>C	XP_016856340.1:p.Tyr738Ser
XM_017000852.1:c.3191A>C	XP_016856341.1:p.Tyr1064Ser
NM_201253.3:c.3056A>C MANE Select	NP_957705.1:p.Tyr1019Ser
NM_001193640.2:c.2720A>C	NP_001180569.1:p.Tyr907Ser
NM_001257965.2:c.2984A>C	NP_001244894.1:p.Tyr995Ser
NR_047563.2:n.3009A>C
NR_047564.2:n.3217A>C
NM_001257966.2:c.2129-681A>C	NP_001244895.1:n.2129-681A>C