Canonical Allele Identifier: CA1337852099

Gene: RAMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237861260A= , CM000664.2:g.237861260A=	GRCh38
NC_000002.11:g.238769903A= , CM000664.1:g.238769903A=	GRCh37
NC_000002.10:g.238434642A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254661.5:c.52+1533A= MANE Select	ENSP00000254661.4:n.52+1533A=
ENST00000254661.4:c.52+1533A=	ENSP00000254661.4:n.52+1533A=
ENST00000403885.1:c.-15+1257A=	ENSP00000386046.1:n.-15+1257A=
ENST00000404910.6:c.-15+2133A=	ENSP00000384688.2:n.-15+2133A=
ENST00000409726.5:c.-76+1533A=	ENSP00000386720.1:n.-76+1533A=
NM_001308353.1:c.-76+1533A=	NP_001295282.1:n.-76+1533A=
NM_005855.2:c.52+1533A=	NP_005846.1:n.52+1533A=
NM_005855.3:c.52+1533A=	NP_005846.1:n.52+1533A=
XM_011510478.1:c.-182+1053A=	XP_011508780.1:n.-182+1053A=
XM_017003152.2:c.-15+1257A=	XP_016858641.1:n.-15+1257A=
XM_017003153.2:c.-15+2133A=	XP_016858642.1:n.-15+2133A=
XM_017003155.1:c.52+1533A=	XP_016858644.1:n.52+1533A=
XM_017003156.2:c.-15+1053A=	XP_016858645.1:n.-15+1053A=
NM_005855.4:c.52+1533A= MANE Select	NP_005846.1:n.52+1533A=
NM_001308353.2:c.-76+1533A=	NP_001295282.1:n.-76+1533A=