Canonical Allele Identifier: CA67897222

Gene: RAMP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237907236T>C , CM000664.2:g.237907236T>C	GRCh38
NC_000002.11:g.238815878T>C , CM000664.1:g.238815878T>C	GRCh37
NC_000002.10:g.238480617T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254661.5:c.192-4292T>C MANE Select	ENSP00000254661.4:n.192-4292T>C
ENST00000254661.4:c.192-4292T>C	ENSP00000254661.4:n.192-4292T>C
ENST00000403885.1:c.126-4292T>C	ENSP00000386046.1:n.126-4292T>C
ENST00000404910.6:c.126-4292T>C	ENSP00000384688.2:n.126-4292T>C
ENST00000409726.5:c.126-4292T>C	ENSP00000386720.1:n.126-4292T>C
NM_001308353.1:c.126-4292T>C	NP_001295282.1:n.126-4292T>C
NM_005855.2:c.192-4292T>C	NP_005846.1:n.192-4292T>C
NM_005855.3:c.192-4292T>C	NP_005846.1:n.192-4292T>C
XM_011510478.1:c.75-4292T>C	XP_011508780.1:n.75-4292T>C
XM_017003152.2:c.126-4292T>C	XP_016858641.1:n.126-4292T>C
XM_017003153.2:c.126-4292T>C	XP_016858642.1:n.126-4292T>C
XM_017003154.1:c.126-4292T>C	XP_016858643.1:n.126-4292T>C
XM_017003156.2:c.126-4292T>C	XP_016858645.1:n.126-4292T>C
NM_005855.4:c.192-4292T>C MANE Select	NP_005846.1:n.192-4292T>C
NM_001308353.2:c.126-4292T>C	NP_001295282.1:n.126-4292T>C