Canonical Allele Identifier: CA1490495004

Gene: AFG2A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122923987T= , CM000666.2:g.122923987T=	GRCh38
NC_000004.11:g.123845142T= , CM000666.1:g.123845142T=	GRCh37
NC_000004.10:g.124064592T=	NCBI36
NG_030404.1:g.4018A=
NG_051570.1:g.5918T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274008.5:c.163+682T= MANE Select	ENSP00000274008.3:n.163+682T=
ENST00000674886.1:n.228+682T=
ENST00000675612.1:c.163+682T=	ENSP00000502453.1:n.163+682T=
ENST00000274008.4:c.163+682T=	ENSP00000274008.3:n.163+682T=
ENST00000422835.2:n.205+682T=
NM_145207.2:c.163+682T=	NP_660208.2:n.163+682T=
XM_005262783.3:c.163+682T=	XP_005262840.1:n.163+682T=
XM_011531678.1:c.163+682T=	XP_011529980.1:n.163+682T=
XM_011531679.1:c.163+682T=	XP_011529981.1:n.163+682T=
NM_001317799.1:c.163+682T=	NP_001304728.1:n.163+682T=
NM_001345856.1:c.163+682T=	NP_001332785.1:n.163+682T=
XM_011531678.2:c.163+682T=	XP_011529980.1:n.163+682T=
XM_011531679.3:c.163+682T=	XP_011529981.1:n.163+682T=
XM_017007825.1:c.163+682T=	XP_016863314.1:n.163+682T=
XM_017007826.1:c.163+682T=	XP_016863315.1:n.163+682T=
XM_017007827.2:c.163+682T=	XP_016863316.1:n.163+682T=
XM_017007828.1:c.-57+704T=	XP_016863317.1:n.-57+704T=
XM_017007830.1:c.163+682T=	XP_016863319.1:n.163+682T=
XR_001741151.1:n.236+682T=
NM_145207.3:c.163+682T= MANE Select	NP_660208.2:n.163+682T=
NM_001317799.2:c.163+682T=	NP_001304728.1:n.163+682T=
NM_001345856.2:c.163+682T=	NP_001332785.1:n.163+682T=