Canonical Allele Identifier: CA540467190

Gene: RAMP1

Linked Data

• dbSNP Id: rs1403861949
• gnomAD v2: 2-238769907-T-G
• gnomAD v3: 2-237861264-T-G
• gnomAD v4: 2-237861264-T-G
• MyVariant Identifiers: chr2:g.238769907T>G (hg19) ; chr2:g.237861264T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237861264T>G , CM000664.2:g.237861264T>G	GRCh38
NC_000002.11:g.238769907T>G , CM000664.1:g.238769907T>G	GRCh37
NC_000002.10:g.238434646T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254661.5:c.52+1537T>G MANE Select	ENSP00000254661.4:n.52+1537T>G
ENST00000254661.4:c.52+1537T>G	ENSP00000254661.4:n.52+1537T>G
ENST00000403885.1:c.-15+1261T>G	ENSP00000386046.1:n.-15+1261T>G
ENST00000404910.6:c.-15+2137T>G	ENSP00000384688.2:n.-15+2137T>G
ENST00000409726.5:c.-76+1537T>G	ENSP00000386720.1:n.-76+1537T>G
NM_001308353.1:c.-76+1537T>G	NP_001295282.1:n.-76+1537T>G
NM_005855.2:c.52+1537T>G	NP_005846.1:n.52+1537T>G
NM_005855.3:c.52+1537T>G	NP_005846.1:n.52+1537T>G
XM_011510478.1:c.-182+1057T>G	XP_011508780.1:n.-182+1057T>G
XM_017003152.2:c.-15+1261T>G	XP_016858641.1:n.-15+1261T>G
XM_017003153.2:c.-15+2137T>G	XP_016858642.1:n.-15+2137T>G
XM_017003155.1:c.52+1537T>G	XP_016858644.1:n.52+1537T>G
XM_017003156.2:c.-15+1057T>G	XP_016858645.1:n.-15+1057T>G
NM_005855.4:c.52+1537T>G MANE Select	NP_005846.1:n.52+1537T>G
NM_001308353.2:c.-76+1537T>G	NP_001295282.1:n.-76+1537T>G