Canonical Allele Identifier: CA2743364526

Gene: ERMAP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42830711_42830712insGGTCCTCGAAACCGCGCATATAGTCCTG , CM000663.2:g.42830711_42830712insGGTCCTCGAAACCGCGCATATAGTCCTG	GRCh38
NC_000001.10:g.43296382_43296383insGGTCCTCGAAACCGCGCATATAGTCCTG , CM000663.1:g.43296382_43296383insGGTCCTCGAAACCGCGCATATAGTCCTG	GRCh37
NC_000001.9:g.43068969_43068970insGGTCCTCGAAACCGCGCATATAGTCCTG	NCBI36
NG_008749.1:g.18607_18608insGGTCCTCGAAACCGCGCATATAGTCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG MANE Select	ENSP00000361595.2:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCT...
ENST00000487556.6:n.452-4327_452-4326insGGTCCTCGAAACCGCGCATATAGTCCTG
ENST00000642150.1:n.273-57_273-56insGGTCCTCGAAACCGCGCATATAGTCCTG
ENST00000643061.1:n.516_517insGGTCCTCGAAACCGCGCATATAGTCCTG
ENST00000647120.1:n.248-4327_248-4326insGGTCCTCGAAACCGCGCATATAGTCCTG
ENST00000328249.3:c.-242_-241insGGTCCTCGAAACCGCGCATATAGTCCTG	ENSP00000332439.3:n.-242_-241insGGTCCTCGAAACCGCGCATATAGTCCTG
ENST00000372514.7:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	ENSP00000361592.3:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCT...
ENST00000372517.6:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	ENSP00000361595.2:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCT...
ENST00000487556.5:n.247-4327_247-4326insGGTCCTCGAAACCGCGCATATAGTCCTG
NM_001017922.1:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	NP_001017922.1:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG
NM_018538.3:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	NP_061008.2:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG
XM_006710313.2:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	XP_006710376.1:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG
XM_011540570.1:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	XP_011538872.1:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG
XM_011540571.1:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	XP_011538873.1:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG
XM_006710313.4:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	XP_006710376.1:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG
XM_011540570.3:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	XP_011538872.1:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG
XM_011540571.3:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	XP_011538873.1:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG
NM_001017922.2:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG MANE Select	NP_001017922.1:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG
NM_018538.4:c.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG	NP_061008.2:n.86-57_86-56insGGTCCTCGAAACCGCGCATATAGTCCTG