Canonical Allele Identifier: CA1337852120

Gene: RAMP1

Linked Data

• dbSNP Id: rs2062130907

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237861309C>T , CM000664.2:g.237861309C>T	GRCh38
NC_000002.11:g.238769952C>T , CM000664.1:g.238769952C>T	GRCh37
NC_000002.10:g.238434691C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254661.5:c.52+1582C>T MANE Select	ENSP00000254661.4:n.52+1582C>T
ENST00000254661.4:c.52+1582C>T	ENSP00000254661.4:n.52+1582C>T
ENST00000403885.1:c.-15+1306C>T	ENSP00000386046.1:n.-15+1306C>T
ENST00000404910.6:c.-15+2182C>T	ENSP00000384688.2:n.-15+2182C>T
ENST00000409726.5:c.-76+1582C>T	ENSP00000386720.1:n.-76+1582C>T
NM_001308353.1:c.-76+1582C>T	NP_001295282.1:n.-76+1582C>T
NM_005855.2:c.52+1582C>T	NP_005846.1:n.52+1582C>T
NM_005855.3:c.52+1582C>T	NP_005846.1:n.52+1582C>T
XM_011510478.1:c.-182+1102C>T	XP_011508780.1:n.-182+1102C>T
XM_017003152.2:c.-15+1306C>T	XP_016858641.1:n.-15+1306C>T
XM_017003153.2:c.-15+2182C>T	XP_016858642.1:n.-15+2182C>T
XM_017003155.1:c.52+1582C>T	XP_016858644.1:n.52+1582C>T
XM_017003156.2:c.-15+1102C>T	XP_016858645.1:n.-15+1102C>T
NM_005855.4:c.52+1582C>T MANE Select	NP_005846.1:n.52+1582C>T
NM_001308353.2:c.-76+1582C>T	NP_001295282.1:n.-76+1582C>T