Canonical Allele Identifier: CA1820592939

Gene: EFR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.131987689A= , CM000670.2:g.131987689A=	GRCh38
NC_000008.10:g.132999936A= , CM000670.1:g.132999936A=	GRCh37
NC_000008.9:g.133069118A=	NCBI36
NG_028112.1:g.88581A=
NG_028112.2:g.88581A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254624.10:c.2052A= MANE Select	ENSP00000254624.5:p.Val684=
ENST00000637848.1:c.2133A=	ENSP00000490312.1:p.Val711=
ENST00000254624.9:c.2052A=	ENSP00000254624.5:p.Val684=
ENST00000519656.1:c.1944A=	ENSP00000428086.1:p.Val648=
ENST00000519920.1:n.477A=
NM_015137.4:c.2052A=	NP_055952.2:p.Val684=
XM_005250849.1:c.1944A=	XP_005250906.1:p.Val648=
XM_011516945.1:c.2121A=	XP_011515247.1:p.Val707=
XR_928314.1:n.2124A=
NM_001323553.1:c.1944A=	NP_001310482.1:p.Val648=
NM_001323554.1:c.1944A=	NP_001310483.1:p.Val648=
NM_001323555.1:c.1944A=	NP_001310484.1:p.Val648=
NM_001323556.1:c.1944A=	NP_001310485.1:p.Val648=
NM_001323557.1:c.1944A=	NP_001310486.1:p.Val648=
NM_001323558.1:c.2052A=	NP_001310487.1:p.Val684=
NM_015137.5:c.2052A=	NP_055952.2:p.Val684=
NR_136615.1:n.2346A=
NR_136616.1:n.2277A=
XR_002956625.1:n.2200A=
NM_015137.6:c.2052A= MANE Select	NP_055952.2:p.Val684=
NM_001323553.2:c.1944A=	NP_001310482.1:p.Val648=
NM_001323554.2:c.1944A=	NP_001310483.1:p.Val648=
NM_001323555.2:c.1944A=	NP_001310484.1:p.Val648=
NM_001323556.2:c.1944A=	NP_001310485.1:p.Val648=
NM_001323557.2:c.1944A=	NP_001310486.1:p.Val648=
NM_001323558.2:c.2052A=	NP_001310487.1:p.Val684=
NR_136615.2:n.2341A=
NR_136616.2:n.2272A=