Canonical Allele Identifier: CA346199911

Gene: EIF2B4

Linked Data

• MyVariant Identifiers: chr2:g.27590685A>C (hg19) ; chr2:g.27367818A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27367818A>C , CM000664.2:g.27367818A>C	GRCh38
NC_000002.11:g.27590685A>C , CM000664.1:g.27590685A>C	GRCh37
NC_000002.10:g.27444189A>C	NCBI36
NG_009305.1:g.7640T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.710T>G MANE Select	ENSP00000233552.6:p.Ile237Ser
ENST00000347454.8:c.710T>G	ENSP00000233552.5:p.Ile237Ser
ENST00000405940.6:c.684T>G	ENSP00000384375.2:p.Asp228Glu
ENST00000417567.1:c.286T>G
ENST00000445933.6:c.707T>G	ENSP00000394397.2:p.Ile236Ser
ENST00000451130.6:c.770T>G	ENSP00000394869.2:p.Ile257Ser
ENST00000475582.5:n.2033T>G
ENST00000493344.6:c.773T>G	ENSP00000429323.1:p.Ile258Ser
ENST00000616081.4:c.701T>G	ENSP00000477710.1:p.Ile234Ser
ENST00000622434.4:c.665T>G	ENSP00000479991.1:p.Ile222Ser
NM_001034116.1:c.710T>G	NP_001029288.1:p.Ile237Ser
NM_015636.3:c.707T>G	NP_056451.3:p.Ile236Ser
NM_172195.3:c.770T>G	NP_751945.2:p.Ile257Ser
XM_005264632.1:c.665T>G	XP_005264689.1:p.Ile222Ser
XM_006712132.1:c.662T>G	XP_006712195.1:p.Ile221Ser
XM_011533147.1:c.92T>G	XP_011531449.1:p.Ile31Ser
NM_001318965.1:c.773T>G	NP_001305894.1:p.Ile258Ser
NM_001318966.1:c.665T>G	NP_001305895.1:p.Ile222Ser
NM_001318967.1:c.617T>G	NP_001305896.1:p.Ile206Ser
NM_001318968.1:c.125T>G	NP_001305897.1:p.Ile42Ser
NM_001318969.1:c.92T>G	NP_001305898.1:p.Ile31Ser
XM_011533147.2:c.92T>G	XP_011531449.1:p.Ile31Ser
NM_001034116.2:c.710T>G MANE Select	NP_001029288.1:p.Ile237Ser
NM_001318965.2:c.773T>G	NP_001305894.1:p.Ile258Ser
NM_001318966.2:c.665T>G	NP_001305895.1:p.Ile222Ser
NM_001318967.2:c.617T>G	NP_001305896.1:p.Ile206Ser
NM_001318968.2:c.125T>G	NP_001305897.1:p.Ile42Ser
NM_001318969.2:c.92T>G	NP_001305898.1:p.Ile31Ser
NM_015636.4:c.707T>G	NP_056451.3:p.Ile236Ser
NM_172195.4:c.770T>G	NP_751945.2:p.Ile257Ser