Canonical Allele Identifier: CA2838367370
Gene: EMG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6974269C>T , CM000674.2:g.6974269C>T GRCh38
NC_000012.11:g.7083431C>T , CM000674.1:g.7083431C>T GRCh37
NC_000012.10:g.6953692C>T NCBI36
NG_021408.1:g.8489C>T
NG_021408.2:g.8489C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599672.6:c.169-70C>T MANE Select ENSP00000470560.1:n.169-70C>T
ENST00000261406.7:c.151-70C>T ENSP00000476966.2:n.151-70C>T
ENST00000539196.2:c.32-70C>T
ENST00000599672.5:c.169-70C>T ENSP00000470560.1:n.169-70C>T
ENST00000607161.5:c.172-70C>T ENSP00000480420.1:n.172-70C>T
ENST00000611981.1:n.180-70C>T
ENST00000620255.1:n.158-70C>T
NM_006331.7:c.169-70C>T NP_006322.4:n.169-70C>T
XM_011520907.1:c.169-70C>T XP_011519209.1:n.169-70C>T
NM_001320049.1:c.169-70C>T NP_001306978.1:n.169-70C>T
NR_135131.1:n.312-70C>T
NM_006331.8:c.169-70C>T MANE Select NP_006322.4:n.169-70C>T
NM_001320049.2:c.169-70C>T NP_001306978.1:n.169-70C>T
NR_135131.2:n.180-70C>T