Canonical Allele Identifier: CA1490671032

Gene: AFG2A

Linked Data

• dbSNP Id: rs1744016322

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.123313836_123313837del , CM000666.2:g.123313836_123313837del	GRCh38
NC_000004.11:g.124234991_124234992del , CM000666.1:g.124234991_124234992del	GRCh37
NC_000004.10:g.124454441_124454442del	NCBI36
NG_051570.1:g.395767_395768del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274008.5:c.2506-52_2506-51del MANE Select	ENSP00000274008.3:n.2506-52_2506-51del
ENST00000675612.1:c.2575-52_2575-51del	ENSP00000502453.1:n.2575-52_2575-51del
ENST00000274008.4:c.2506-52_2506-51del	ENSP00000274008.3:n.2506-52_2506-51del
NM_145207.2:c.2506-52_2506-51del	NP_660208.2:n.2506-52_2506-51del
XM_005262783.3:c.2503-52_2503-51del	XP_005262840.1:n.2503-52_2503-51del
XM_011531678.1:c.2575-52_2575-51del	XP_011529980.1:n.2575-52_2575-51del
NM_001345856.1:c.2503-52_2503-51del	NP_001332785.1:n.2503-52_2503-51del
XM_011531678.2:c.2575-52_2575-51del	XP_011529980.1:n.2575-52_2575-51del
XM_017007825.1:c.2578-52_2578-51del	XP_016863314.1:n.2578-52_2578-51del
XM_017007828.1:c.2284-52_2284-51del	XP_016863317.1:n.2284-52_2284-51del
XM_017007829.1:c.2122-52_2122-51del	XP_016863318.1:n.2122-52_2122-51del
XR_001741151.1:n.2664-52_2664-51del
NM_145207.3:c.2506-52_2506-51del MANE Select	NP_660208.2:n.2506-52_2506-51del
NM_001345856.2:c.2503-52_2503-51del	NP_001332785.1:n.2503-52_2503-51del