Canonical Allele Identifier: CA344037913

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396969G>T (hg19) ; chr1:g.197427839G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427839G>T , CM000663.2:g.197427839G>T	GRCh38
NC_000001.10:g.197396969G>T , CM000663.1:g.197396969G>T	GRCh37
NC_000001.9:g.195663592G>T	NCBI36
NG_008483.1:g.164562G>T
NG_008483.2:g.231378G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.2514G>T MANE Select	ENSP00000356370.3:p.Lys838Asn
ENST00000638467.1:c.2514G>T	ENSP00000491102.1:p.Lys838Asn
ENST00000681519.1:c.1395G>T	ENSP00000505267.1:p.Lys465Asn
ENST00000367397.1:c.657G>T	ENSP00000356367.1:p.Lys219Asn
ENST00000367399.6:c.2178G>T	ENSP00000356369.2:p.Lys726Asn
ENST00000367400.7:c.2514G>T	ENSP00000356370.3:p.Lys838Asn
ENST00000484075.5:c.2514G>T	ENSP00000433932.1:p.Lys838Asn
ENST00000535699.5:c.2307G>T	ENSP00000438786.1:p.Lys769Asn
ENST00000538660.5:c.2128+5883G>T	ENSP00000438091.1:n.2128+5883G>T
NM_001193640.1:c.2178G>T	NP_001180569.1:p.Lys726Asn
NM_001257965.1:c.2307G>T	NP_001244894.1:p.Lys769Asn
NM_001257966.1:c.2128+5883G>T	NP_001244895.1:n.2128+5883G>T
NM_201253.2:c.2514G>T	NP_957705.1:p.Lys838Asn
NR_047563.1:n.2515G>T
NR_047564.1:n.2723G>T
XM_011509365.1:c.2514G>T	XP_011507667.1:p.Lys838Asn
XM_011509366.1:c.2514G>T	XP_011507668.1:p.Lys838Asn
XM_011509367.1:c.2514G>T	XP_011507669.1:p.Lys838Asn
XM_011509368.1:c.1932G>T	XP_011507670.1:p.Lys644Asn
XM_011509369.1:c.957G>T	XP_011507671.1:p.Lys319Asn
XM_011509365.2:c.2514G>T	XP_011507667.1:p.Lys838Asn
XM_011509369.2:c.957G>T	XP_011507671.1:p.Lys319Asn
XM_017000851.1:c.1671G>T	XP_016856340.1:p.Lys557Asn
XM_017000852.1:c.2514G>T	XP_016856341.1:p.Lys838Asn
NM_201253.3:c.2514G>T MANE Select	NP_957705.1:p.Lys838Asn
NM_001193640.2:c.2178G>T	NP_001180569.1:p.Lys726Asn
NM_001257965.2:c.2307G>T	NP_001244894.1:p.Lys769Asn
NR_047563.2:n.2467G>T
NR_047564.2:n.2675G>T
NM_001257966.2:c.2128+5883G>T	NP_001244895.1:n.2128+5883G>T