Canonical Allele Identifier: CA360511606

Gene: ERAP2 ERAP1

Linked Data

• MyVariant Identifiers: chr5:g.96235870G>C (hg19) ; chr5:g.96900166G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96900166G>C , CM000667.2:g.96900166G>C	GRCh38
NC_000005.9:g.96235870G>C , CM000667.1:g.96235870G>C	GRCh37
NC_000005.8:g.96261626G>C	NCBI36
NG_027839.2:g.40818C>G
NG_051092.1:g.29228G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510373.6:c.1549G>C (ERAP2)	ENSP00000421175.2:p.Asp517His
ENST00000437043.8:c.1549G>C (ERAP2) MANE Select	ENSP00000400376.3:p.Asp517His
ENST00000379904.8:c.1414G>C (ERAP2)	ENSP00000369235.4:p.Asp472His
ENST00000437043.7:c.1549G>C (ERAP2)	ENSP00000400376.3:p.Asp517His
ENST00000510373.5:c.1549G>C (ERAP2)	ENSP00000421175.1:p.Asp517His
ENST00000513084.5:c.1549G>C (ERAP2)	ENSP00000421849.1:p.Asp517His
ENST00000513368.1:n.338G>C (ERAP2)
ENST00000515095.5:n.460G>C (ERAP2)
ENST00000515387.1:n.280G>C (ERAP2)
NM_001130140.1:c.1549G>C (ERAP2)	NP_001123612.1:p.Asp517His
NM_022350.3:c.1549G>C (ERAP2)	NP_071745.1:p.Asp517His
XM_011543480.1:c.-705-26494C>G (ERAP1)	XP_011541782.1:n.-705-26494C>G
XM_011543481.1:c.-702-26494C>G (ERAP1)	XP_011541783.1:n.-702-26494C>G
XM_011543482.1:c.-709-26494C>G (ERAP1)	XP_011541784.1:n.-709-26494C>G
XM_011543483.1:c.-872-26494C>G (ERAP1)	XP_011541785.1:n.-872-26494C>G
XM_011543484.1:c.-701-26494C>G (ERAP1)	XP_011541786.1:n.-701-26494C>G
XM_011543485.1:c.-521-26494C>G (ERAP1)	XP_011541787.1:n.-521-26494C>G
XM_011543486.1:c.-705-26494C>G (ERAP1)	XP_011541788.1:n.-705-26494C>G
XM_011543487.1:c.-705-26494C>G (ERAP1)	XP_011541789.1:n.-705-26494C>G
XM_011543544.1:c.1504-1340G>C (ERAP2)	XP_011541846.1:n.1504-1340G>C
XR_948283.1:n.1732G>C (ERAP2)
NM_001130140.2:c.1549G>C (ERAP2)	NP_001123612.1:p.Asp517His
NM_001329229.1:c.1414G>C (ERAP2)	NP_001316158.1:p.Asp472His
NM_022350.4:c.1549G>C (ERAP2)	NP_071745.1:p.Asp517His
NR_137637.1:n.2260G>C (ERAP2)
XM_011543480.2:c.-705-26494C>G (ERAP1)	XP_011541782.1:n.-705-26494C>G
XM_011543481.2:c.-702-26494C>G (ERAP1)	XP_011541783.1:n.-702-26494C>G
XM_011543484.2:c.-701-26494C>G (ERAP1)	XP_011541786.1:n.-701-26494C>G
XM_011543485.2:c.-521-26494C>G (ERAP1)	XP_011541787.1:n.-521-26494C>G
XM_011543486.3:c.-705-26494C>G (ERAP1)	XP_011541788.1:n.-705-26494C>G
XM_011543544.2:c.1504-1340G>C (ERAP2)	XP_011541846.1:n.1504-1340G>C
XM_017009581.1:c.-547-26788C>G (ERAP1)	XP_016865070.1:n.-547-26788C>G
XM_024446113.1:c.-544-26788C>G (ERAP1)	XP_024301881.1:n.-544-26788C>G
XR_001742179.2:n.1717G>C (ERAP2)
NM_022350.5:c.1549G>C (ERAP2) MANE Select	NP_071745.1:p.Asp517His