Canonical Allele Identifier: CA2035843919
Gene: SLC11A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.50992885A= , CM000674.2:g.50992885A= GRCh38
NC_000012.11:g.51386668A= , CM000674.1:g.51386668A= GRCh37
NC_000012.10:g.49672935A= NCBI36
NG_021139.1:g.40391T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394904.9:c.1209T= ENSP00000378364.3:p.Ile403=
ENST00000545993.7:c.1110T= ENSP00000442810.2:p.Ile370=
ENST00000547688.7:c.1209T= ENSP00000449200.2:p.Ile403=
ENST00000642227.1:c.*707T= ENSP00000494696.1:n.*707T=
ENST00000643123.1:n.174T=
ENST00000643884.1:c.1158T= ENSP00000493633.1:p.Ile386=
ENST00000644495.1:c.1122T= ENSP00000494107.1:p.Ile374=
ENST00000646264.1:c.692T=
ENST00000646740.1:c.*296T= ENSP00000494001.1:n.*296T=
ENST00000262051.11:c.1122T= ENSP00000262051.7:p.Ile374=
ENST00000262052.9:c.1122T= MANE Select ENSP00000262052.5:p.Ile374=
ENST00000394904.7:c.1209T= ENSP00000378364.3:p.Ile403=
ENST00000541174.6:c.1122T= ENSP00000444542.2:p.Ile374=
ENST00000545993.6:c.1110T= ENSP00000442810.2:p.Ile370=
ENST00000546636.5:c.1122T= ENSP00000449008.1:p.Ile374=
ENST00000546743.5:c.885T= ENSP00000446914.1:p.Ile295=
ENST00000547198.5:c.1122T= ENSP00000446769.1:p.Ile374=
ENST00000547688.5:c.1209T= ENSP00000449200.1:p.Ile403=
ENST00000550782.5:n.594T=
ENST00000551231.1:n.260T=
NM_000617.2:c.1122T= NP_000608.1:p.Ile374=
NM_001174125.1:c.1209T= NP_001167596.1:p.Ile403=
NM_001174126.1:c.1122T= NP_001167597.1:p.Ile374=
NM_001174127.1:c.1122T= NP_001167598.1:p.Ile374=
NM_001174128.1:c.1122T= NP_001167599.1:p.Ile374=
NM_001174129.1:c.1122T= NP_001167600.1:p.Ile374=
NM_001174130.1:c.1110T= NP_001167601.1:p.Ile370=
NR_033421.1:n.1187T=
NR_033422.1:n.1262T=
XM_005268911.2:c.1209T= XP_005268968.1:p.Ile403=
XM_005268912.3:c.1110T= XP_005268969.1:p.Ile370=
XM_005268913.2:c.1011T= XP_005268970.1:p.Ile337=
XM_005268914.2:c.1011T= XP_005268971.1:p.Ile337=
XM_011538404.1:c.1122T= XP_011536706.1:p.Ile374=
XM_011538405.1:c.1122T= XP_011536707.1:p.Ile374=
XM_011538406.1:c.885T= XP_011536708.1:p.Ile295=
XR_429104.1:n.1319T=
XR_944555.1:n.1319T=
XM_005268911.3:c.1209T= XP_005268968.1:p.Ile403=
XM_005268912.5:c.1110T= XP_005268969.1:p.Ile370=
XM_011538404.3:c.1122T= XP_011536706.1:p.Ile374=
XM_011538405.3:c.1122T= XP_011536707.1:p.Ile374=
XM_017019355.2:c.1122T= XP_016874844.1:p.Ile374=
XM_017019356.2:c.885T= XP_016874845.1:p.Ile295=
XR_001748720.1:n.1319T=
XR_001748721.2:n.1237T=
XR_001748722.2:n.1245T=
XR_001748723.2:n.1245T=
NM_000617.3:c.1122T= MANE Select NP_000608.1:p.Ile374=
NM_001174125.2:c.1209T= NP_001167596.1:p.Ile403=
NM_001174128.2:c.1122T= NP_001167599.1:p.Ile374=
NM_001174130.2:c.1110T= NP_001167601.1:p.Ile370=
NR_033421.2:n.1155T=
NR_033422.2:n.1230T=
NM_001174126.2:c.1122T= NP_001167597.1:p.Ile374=
NM_001174127.2:c.1122T= NP_001167598.1:p.Ile374=
NM_001379446.1:c.1209T= NP_001366375.1:p.Ile403=
NM_001379447.1:c.1122T= NP_001366376.1:p.Ile374=
NM_001379448.1:c.1110T= NP_001366377.1:p.Ile370=
NM_001379455.1:c.1209T= NP_001366384.1:p.Ile403=
NR_166668.1:n.1235T=
NR_166669.1:n.1230T=
NR_166670.1:n.1235T=