Canonical Allele Identifier: CA1589140771

Gene: TCERG1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146458962C= , CM000667.2:g.146458962C=	GRCh38
NC_000005.9:g.145838525C= , CM000667.1:g.145838525C=	GRCh37
NC_000005.8:g.145818718C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707167.1:c.517C=	ENSP00000516769.1:p.Leu173=
ENST00000679501.2:c.517C= MANE Select	ENSP00000505217.1:p.Leu173=
ENST00000394421.7:c.517C=	ENSP00000377943.2:p.Leu173=
ENST00000679501.1:c.517C=	ENSP00000505217.1:p.Leu173=
ENST00000296702.9:c.517C=	ENSP00000296702.5:p.Leu173=
ENST00000394421.6:c.517C=	ENSP00000377943.2:p.Leu173=
ENST00000507175.5:n.556C=
ENST00000549332.1:c.517C=	ENSP00000450414.1:p.Leu173=
NM_001040006.1:c.517C=	NP_001035095.1:p.Leu173=
NM_006706.3:c.517C=	NP_006697.2:p.Leu173=
XM_005268365.1:c.517C=	XP_005268422.1:p.Leu173=
XM_011537545.1:c.517C=	XP_011535847.1:p.Leu173=
XM_011537546.1:c.517C=	XP_011535848.1:p.Leu173=
XM_011537547.1:c.517C=	XP_011535849.1:p.Leu173=
XM_011537548.1:c.517C=	XP_011535850.1:p.Leu173=
XM_011537549.1:c.517C=	XP_011535851.1:p.Leu173=
XR_944306.1:n.556C=
XR_944307.1:n.556C=
XM_005268365.3:c.517C=	XP_005268422.1:p.Leu173=
XM_017008977.2:c.517C=	XP_016864466.1:p.Leu173=
XM_017008978.2:c.517C=	XP_016864467.1:p.Leu173=
XM_017008979.2:c.517C=	XP_016864468.1:p.Leu173=
XM_017008980.2:c.517C=	XP_016864469.1:p.Leu173=
XM_017008982.2:c.-385C=	XP_016864471.1:n.-385C=
XM_017008983.2:c.-385C=	XP_016864472.1:n.-385C=
XM_017008984.2:c.517C=	XP_016864473.1:p.Leu173=
XM_017008985.2:c.517C=	XP_016864474.1:p.Leu173=
XM_024454341.1:c.-385C=	XP_024310109.1:n.-385C=
XM_024454342.1:c.-385C=	XP_024310110.1:n.-385C=
XR_001741980.2:n.537C=
XR_001741981.2:n.537C=
XR_001741982.2:n.537C=
XR_001741983.2:n.537C=
XR_001741984.2:n.537C=
XR_001741985.2:n.537C=
XR_002959840.1:n.537C=
NM_001040006.2:c.517C=	NP_001035095.1:p.Leu173=
NM_006706.4:c.517C=	NP_006697.2:p.Leu173=
NM_001382548.1:c.517C= MANE Select	NP_001369477.1:p.Leu173=
NM_001400077.1:c.517C=	NP_001387006.1:p.Leu173=
NM_001400082.1:c.460C=	NP_001387011.1:p.Leu154=
NM_001400083.1:c.517C=	NP_001387012.1:p.Leu173=
NM_001400084.1:c.517C=	NP_001387013.1:p.Leu173=
NM_001400085.1:c.517C=	NP_001387014.1:p.Leu173=
NM_001400092.1:c.457C=	NP_001387021.1:p.Leu153=
NM_001400093.1:c.517C=	NP_001387022.1:p.Leu173=
NM_001400094.1:c.517C=	NP_001387023.1:p.Leu173=
NM_001400095.1:c.517C=	NP_001387024.1:p.Leu173=
NM_001400096.1:c.517C=	NP_001387025.1:p.Leu173=
NM_001400097.1:c.517C=	NP_001387026.1:p.Leu173=
NM_001400098.1:c.517C=	NP_001387027.1:p.Leu173=
NM_001400099.1:c.517C=	NP_001387028.1:p.Leu173=
NR_174389.1:n.534C=
NR_174390.1:n.534C=
NR_174391.1:n.534C=
NR_174406.1:n.537C=
NR_174407.1:n.537C=
NR_174408.1:n.534C=
NR_174409.1:n.534C=
NR_174410.1:n.534C=
NR_174411.1:n.534C=
NR_174412.1:n.534C=
NR_174413.1:n.534C=
NR_174414.1:n.624C=
NR_174415.1:n.534C=
NR_174416.1:n.534C=
NR_174417.1:n.534C=
NR_174418.1:n.534C=
NR_174419.1:n.534C=
NR_174420.1:n.534C=
NR_174421.1:n.534C=
NR_174422.1:n.534C=
NR_174423.1:n.534C=
NR_174424.1:n.534C=
NR_174425.1:n.534C=
NR_174426.1:n.534C=
NR_174427.1:n.534C=
NR_174428.1:n.534C=
NR_174429.1:n.534C=
NR_174430.1:n.534C=
NR_174431.1:n.534C=
NR_174432.1:n.534C=
NR_174433.1:n.534C=
NR_174434.1:n.534C=
NR_174435.1:n.534C=
NR_174436.1:n.534C=
NR_174437.1:n.534C=
NR_174438.1:n.534C=
NR_174439.1:n.534C=
NR_174440.1:n.534C=
NR_174441.1:n.534C=
NR_174442.1:n.534C=
NR_174443.1:n.534C=
NR_174444.1:n.534C=
NR_174445.1:n.534C=
NR_174446.1:n.534C=
NR_174447.1:n.534C=
NR_174448.1:n.534C=
NR_174449.1:n.534C=
NR_174450.1:n.534C=
NR_174451.1:n.534C=
NR_174452.1:n.534C=
NR_174453.1:n.534C=
NR_174454.1:n.534C=