Canonical Allele Identifier: CA383682485
Gene: EMG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6974348A>G , CM000674.2:g.6974348A>G GRCh38
NC_000012.11:g.7083510A>G , CM000674.1:g.7083510A>G GRCh37
NC_000012.10:g.6953771A>G NCBI36
NG_021408.1:g.8568A>G
NG_021408.2:g.8568A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000599672.6:c.178A>G MANE Select ENSP00000470560.1:p.Thr60Ala
ENST00000261406.7:c.160A>G ENSP00000476966.2:p.Thr54Ala
ENST00000539196.2:c.41A>G
ENST00000599672.5:c.178A>G ENSP00000470560.1:p.Thr60Ala
ENST00000607161.5:c.181A>G ENSP00000480420.1:p.Thr61Ala
ENST00000611981.1:n.189A>G
ENST00000620255.1:n.167A>G
NM_006331.7:c.178A>G NP_006322.4:p.Thr60Ala
XM_011520907.1:c.178A>G XP_011519209.1:p.Thr60Ala
NM_001320049.1:c.178A>G NP_001306978.1:p.Thr60Ala
NR_135131.1:n.321A>G
NM_006331.8:c.178A>G MANE Select NP_006322.4:p.Thr60Ala
NM_001320049.2:c.178A>G NP_001306978.1:p.Thr60Ala
NR_135131.2:n.189A>G