Canonical Allele Identifier: CA11050934

Gene: RAMP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237881216C>A , CM000664.2:g.237881216C>A	GRCh38
NC_000002.11:g.238789858C>A , CM000664.1:g.238789858C>A	GRCh37
NC_000002.10:g.238454597C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254661.5:c.191+3854C>A MANE Select	ENSP00000254661.4:n.191+3854C>A
ENST00000254661.4:c.191+3854C>A	ENSP00000254661.4:n.191+3854C>A
ENST00000403885.1:c.125+3854C>A	ENSP00000386046.1:n.125+3854C>A
ENST00000404910.6:c.125+3854C>A	ENSP00000384688.2:n.125+3854C>A
ENST00000409726.5:c.125+3854C>A	ENSP00000386720.1:n.125+3854C>A
NM_001308353.1:c.125+3854C>A	NP_001295282.1:n.125+3854C>A
NM_005855.2:c.191+3854C>A	NP_005846.1:n.191+3854C>A
NM_005855.3:c.191+3854C>A	NP_005846.1:n.191+3854C>A
XM_011510478.1:c.74+3108C>A	XP_011508780.1:n.74+3108C>A
XM_017003152.2:c.125+3854C>A	XP_016858641.1:n.125+3854C>A
XM_017003153.2:c.125+3854C>A	XP_016858642.1:n.125+3854C>A
XM_017003154.1:c.125+3854C>A	XP_016858643.1:n.125+3854C>A
XM_017003156.2:c.125+3854C>A	XP_016858645.1:n.125+3854C>A
NM_005855.4:c.191+3854C>A MANE Select	NP_005846.1:n.191+3854C>A
NM_001308353.2:c.125+3854C>A	NP_001295282.1:n.125+3854C>A