Canonical Allele Identifier: CA15291362

Gene: ROPN1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123986995G>A , CM000665.2:g.123986995G>A	GRCh38
NC_000003.11:g.123705842G>A , CM000665.1:g.123705842G>A	GRCh37
NC_000003.10:g.125188532G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405845.8:c.-13+4927C>T MANE Select	ENSP00000385919.3:n.-13+4927C>T
ENST00000184183.8:c.-170+4186C>T	ENSP00000184183.4:n.-170+4186C>T
ENST00000405845.7:c.-13+4927C>T	ENSP00000385919.3:n.-13+4927C>T
ENST00000459660.5:c.-59+5049C>T	ENSP00000420590.1:n.-59+5049C>T
ENST00000460743.5:c.-59+4186C>T	ENSP00000420310.1:n.-59+4186C>T
ENST00000467907.5:c.-170+4927C>T	ENSP00000417067.1:n.-170+4927C>T
ENST00000479867.1:c.-13+4927C>T	ENSP00000420567.1:n.-13+4927C>T
ENST00000484329.1:c.-170+4927C>T	ENSP00000419205.1:n.-170+4927C>T
ENST00000487124.1:n.162+4927C>T
ENST00000495093.1:c.-124+4927C>T	ENSP00000417379.1:n.-124+4927C>T
ENST00000496145.5:c.-59+4927C>T	ENSP00000418931.1:n.-59+4927C>T
NM_017578.2:c.-170+4186C>T	NP_060048.2:n.-170+4186C>T
XM_005247549.2:c.-13+4927C>T	XP_005247606.1:n.-13+4927C>T
XM_005247551.3:c.-161+4927C>T	XP_005247608.1:n.-161+4927C>T
XM_011512933.1:c.-59+4927C>T	XP_011511235.1:n.-59+4927C>T
XM_011512934.1:c.-170+4927C>T	XP_011511236.1:n.-170+4927C>T
XM_011512935.1:c.-124+4927C>T	XP_011511237.1:n.-124+4927C>T
XM_011512936.1:c.-13+4927C>T	XP_011511238.1:n.-13+4927C>T
NM_001317774.1:c.-13+4927C>T	NP_001304703.1:n.-13+4927C>T
NM_001317775.1:c.-161+4927C>T	NP_001304704.1:n.-161+4927C>T
NM_017578.3:c.-170+4186C>T	NP_060048.2:n.-170+4186C>T
NR_133916.1:n.249+4927C>T
NR_133917.1:n.127+5049C>T
NR_133918.1:n.249+4927C>T
NR_133919.1:n.249+4927C>T
XM_011512933.2:c.-59+4927C>T	XP_011511235.1:n.-59+4927C>T
XM_011512934.2:c.-170+4927C>T	XP_011511236.1:n.-170+4927C>T
NM_017578.4:c.-170+4186C>T	NP_060048.2:n.-170+4186C>T
NM_001317774.2:c.-13+4927C>T MANE Select	NP_001304703.1:n.-13+4927C>T
NM_001317775.2:c.-161+4927C>T	NP_001304704.1:n.-161+4927C>T
NM_001394217.1:c.-59+4927C>T	NP_001381146.1:n.-59+4927C>T
NM_001394218.1:c.-170+4927C>T	NP_001381147.1:n.-170+4927C>T
NM_001394219.1:c.-59+4186C>T	NP_001381148.1:n.-59+4186C>T
NM_017578.5:c.-170+4186C>T	NP_060048.2:n.-170+4186C>T
NR_133916.2:n.203+4927C>T
NR_133917.2:n.81+5049C>T
NR_133918.2:n.203+4927C>T
NR_133919.2:n.203+4927C>T
NR_172091.1:n.203+4927C>T