Canonical Allele Identifier: CA344043889

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197403943G>T (hg19) ; chr1:g.197434813G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434813G>T , CM000663.2:g.197434813G>T	GRCh38
NC_000001.10:g.197403943G>T , CM000663.1:g.197403943G>T	GRCh37
NC_000001.9:g.195670566G>T	NCBI36
NG_008483.1:g.171536G>T
NG_008483.2:g.238352G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2950G>T MANE Select	ENSP00000356370.3:p.Asp984Tyr
ENST00000638467.1:c.2950G>T	ENSP00000491102.1:p.Asp984Tyr
ENST00000681519.1:c.1831G>T	ENSP00000505267.1:p.Asp611Tyr
ENST00000367397.1:c.1093G>T	ENSP00000356367.1:p.Asp365Tyr
ENST00000367399.6:c.2614G>T	ENSP00000356369.2:p.Asp872Tyr
ENST00000367400.7:c.2950G>T	ENSP00000356370.3:p.Asp984Tyr
ENST00000484075.5:c.2950G>T	ENSP00000433932.1:p.Asp984Tyr
ENST00000535699.5:c.2878G>T	ENSP00000438786.1:p.Asp960Tyr
ENST00000538660.5:c.2129-787G>T	ENSP00000438091.1:n.2129-787G>T
NM_001193640.1:c.2614G>T	NP_001180569.1:p.Asp872Tyr
NM_001257965.1:c.2878G>T	NP_001244894.1:p.Asp960Tyr
NM_001257966.1:c.2129-787G>T	NP_001244895.1:n.2129-787G>T
NM_201253.2:c.2950G>T	NP_957705.1:p.Asp984Tyr
NR_047563.1:n.2951G>T
NR_047564.1:n.3159G>T
XM_011509365.1:c.2950G>T	XP_011507667.1:p.Asp984Tyr
XM_011509366.1:c.2950G>T	XP_011507668.1:p.Asp984Tyr
XM_011509367.1:c.2950G>T	XP_011507669.1:p.Asp984Tyr
XM_011509368.1:c.2368G>T	XP_011507670.1:p.Asp790Tyr
XM_011509369.1:c.1393G>T	XP_011507671.1:p.Asp465Tyr
XM_011509365.2:c.2950G>T	XP_011507667.1:p.Asp984Tyr
XM_011509369.2:c.1393G>T	XP_011507671.1:p.Asp465Tyr
XM_017000851.1:c.2107G>T	XP_016856340.1:p.Asp703Tyr
XM_017000852.1:c.3085G>T	XP_016856341.1:p.Asp1029Tyr
NM_201253.3:c.2950G>T MANE Select	NP_957705.1:p.Asp984Tyr
NM_001193640.2:c.2614G>T	NP_001180569.1:p.Asp872Tyr
NM_001257965.2:c.2878G>T	NP_001244894.1:p.Asp960Tyr
NR_047563.2:n.2903G>T
NR_047564.2:n.3111G>T
NM_001257966.2:c.2129-787G>T	NP_001244895.1:n.2129-787G>T