Canonical Allele Identifier: CA425409825

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587450C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364583C>A , CM000664.2:g.27364583C>A	GRCh38
NC_000002.11:g.27587450C>A , CM000664.1:g.27587450C>A	GRCh37
NC_000002.10:g.27440954C>A	NCBI36
NG_009305.1:g.10875G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000347454.9:c.1389G>T (EIF2B4) MANE Select	ENSP00000233552.6:p.Leu463=
ENST00000347454.8:c.1389G>T (EIF2B4)	ENSP00000233552.5:p.Leu463=
ENST00000405940.6:c.*655G>T (EIF2B4)	ENSP00000384375.2:n.*655G>T
ENST00000445933.6:c.1386G>T (EIF2B4)	ENSP00000394397.2:p.Leu462=
ENST00000451130.6:c.1449G>T (EIF2B4)	ENSP00000394869.2:p.Leu483=
ENST00000478311.1:n.382G>T (EIF2B4)
ENST00000493344.6:c.1452G>T (EIF2B4)	ENSP00000429323.1:p.Leu484=
ENST00000616081.4:c.1380G>T (EIF2B4)	ENSP00000477710.1:p.Leu460=
ENST00000622434.4:c.*655G>T (EIF2B4)	ENSP00000479991.1:n.*655G>T
NM_001034116.1:c.1389G>T (EIF2B4)	NP_001029288.1:p.Leu463=
NM_015636.3:c.1386G>T (EIF2B4)	NP_056451.3:p.Leu462=
NM_172195.3:c.1449G>T (EIF2B4)	NP_751945.2:p.Leu483=
XM_005264632.1:c.1344G>T (EIF2B4)	XP_005264689.1:p.Leu448=
XM_006712132.1:c.1341G>T (EIF2B4)	XP_006712195.1:p.Leu447=
XM_011533147.1:c.771G>T (EIF2B4)	XP_011531449.1:p.Leu257=
XR_939868.1:n.1772-2841C>A (GTF3C2-AS2)
NM_001318965.1:c.1452G>T (EIF2B4)	NP_001305894.1:p.Leu484=
NM_001318966.1:c.1344G>T (EIF2B4)	NP_001305895.1:p.Leu448=
NM_001318967.1:c.1296G>T (EIF2B4)	NP_001305896.1:p.Leu432=
NM_001318968.1:c.804G>T (EIF2B4)	NP_001305897.1:p.Leu268=
NM_001318969.1:c.771G>T (EIF2B4)	NP_001305898.1:p.Leu257=
XM_011533147.2:c.771G>T (EIF2B4)	XP_011531449.1:p.Leu257=
NM_001034116.2:c.1389G>T (EIF2B4) MANE Select	NP_001029288.1:p.Leu463=
NM_001318965.2:c.1452G>T (EIF2B4)	NP_001305894.1:p.Leu484=
NM_001318966.2:c.1344G>T (EIF2B4)	NP_001305895.1:p.Leu448=
NM_001318967.2:c.1296G>T (EIF2B4)	NP_001305896.1:p.Leu432=
NM_001318968.2:c.804G>T (EIF2B4)	NP_001305897.1:p.Leu268=
NM_001318969.2:c.771G>T (EIF2B4)	NP_001305898.1:p.Leu257=
NM_015636.4:c.1386G>T (EIF2B4)	NP_056451.3:p.Leu462=
NM_172195.4:c.1449G>T (EIF2B4)	NP_751945.2:p.Leu483=