Canonical Allele Identifier: CA344037059

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396822T>A (hg19) ; chr1:g.197427692T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427692T>A , CM000663.2:g.197427692T>A	GRCh38
NC_000001.10:g.197396822T>A , CM000663.1:g.197396822T>A	GRCh37
NC_000001.9:g.195663445T>A	NCBI36
NG_008483.1:g.164415T>A
NG_008483.2:g.231231T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2367T>A MANE Select	ENSP00000356370.3:p.Asn789Lys
ENST00000638467.1:c.2367T>A	ENSP00000491102.1:p.Asn789Lys
ENST00000681519.1:c.1248T>A	ENSP00000505267.1:p.Asn416Lys
ENST00000367397.1:c.510T>A	ENSP00000356367.1:p.Asn170Lys
ENST00000367399.6:c.2031T>A	ENSP00000356369.2:p.Asn677Lys
ENST00000367400.7:c.2367T>A	ENSP00000356370.3:p.Asn789Lys
ENST00000480086.2:n.268T>A
ENST00000484075.5:c.2367T>A	ENSP00000433932.1:p.Asn789Lys
ENST00000535699.5:c.2160T>A	ENSP00000438786.1:p.Asn720Lys
ENST00000538660.5:c.2128+5736T>A	ENSP00000438091.1:n.2128+5736T>A
NM_001193640.1:c.2031T>A	NP_001180569.1:p.Asn677Lys
NM_001257965.1:c.2160T>A	NP_001244894.1:p.Asn720Lys
NM_001257966.1:c.2128+5736T>A	NP_001244895.1:n.2128+5736T>A
NM_201253.2:c.2367T>A	NP_957705.1:p.Asn789Lys
NR_047563.1:n.2368T>A
NR_047564.1:n.2576T>A
XM_011509365.1:c.2367T>A	XP_011507667.1:p.Asn789Lys
XM_011509366.1:c.2367T>A	XP_011507668.1:p.Asn789Lys
XM_011509367.1:c.2367T>A	XP_011507669.1:p.Asn789Lys
XM_011509368.1:c.1785T>A	XP_011507670.1:p.Asn595Lys
XM_011509369.1:c.810T>A	XP_011507671.1:p.Asn270Lys
XM_011509365.2:c.2367T>A	XP_011507667.1:p.Asn789Lys
XM_011509369.2:c.810T>A	XP_011507671.1:p.Asn270Lys
XM_017000851.1:c.1524T>A	XP_016856340.1:p.Asn508Lys
XM_017000852.1:c.2367T>A	XP_016856341.1:p.Asn789Lys
NM_201253.3:c.2367T>A MANE Select	NP_957705.1:p.Asn789Lys
NM_001193640.2:c.2031T>A	NP_001180569.1:p.Asn677Lys
NM_001257965.2:c.2160T>A	NP_001244894.1:p.Asn720Lys
NR_047563.2:n.2320T>A
NR_047564.2:n.2528T>A
NM_001257966.2:c.2128+5736T>A	NP_001244895.1:n.2128+5736T>A