Canonical Allele Identifier: CA2014342490

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974260_6974261delinsTG , CM000674.2:g.6974260_6974261delinsTG	GRCh38
NC_000012.11:g.7083422_7083423delinsTG , CM000674.1:g.7083422_7083423delinsTG	GRCh37
NC_000012.10:g.6953683_6953684delinsTG	NCBI36
NG_021408.1:g.8480_8481delinsTG
NG_021408.2:g.8480_8481delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.169-79_169-78delinsTG MANE Select	ENSP00000470560.1:n.169-79_169-78delinsTG
ENST00000261406.7:c.151-79_151-78delinsTG	ENSP00000476966.2:n.151-79_151-78delinsTG
ENST00000539196.2:c.32-79_32-78delinsTG
ENST00000599672.5:c.169-79_169-78delinsTG	ENSP00000470560.1:n.169-79_169-78delinsTG
ENST00000607161.5:c.172-79_172-78delinsTG	ENSP00000480420.1:n.172-79_172-78delinsTG
ENST00000611981.1:n.180-79_180-78delinsTG
ENST00000620255.1:n.158-79_158-78delinsTG
NM_006331.7:c.169-79_169-78delinsTG	NP_006322.4:n.169-79_169-78delinsTG
XM_011520907.1:c.169-79_169-78delinsTG	XP_011519209.1:n.169-79_169-78delinsTG
NM_001320049.1:c.169-79_169-78delinsTG	NP_001306978.1:n.169-79_169-78delinsTG
NR_135131.1:n.312-79_312-78delinsTG
NM_006331.8:c.169-79_169-78delinsTG MANE Select	NP_006322.4:n.169-79_169-78delinsTG
NM_001320049.2:c.169-79_169-78delinsTG	NP_001306978.1:n.169-79_169-78delinsTG
NR_135131.2:n.180-79_180-78delinsTG