Canonical Allele Identifier: CA380680021

Gene: TMEM138

Linked Data

• MyVariant Identifiers: chr11:g.61135393A>C (hg19) ; chr11:g.61367921A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61367921A>C , CM000673.2:g.61367921A>C	GRCh38
NC_000011.9:g.61135393A>C , CM000673.1:g.61135393A>C	GRCh37
NC_000011.8:g.60891969A>C	NCBI36
NG_032581.1:g.10921A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000451389.7:c.301-2A>C	ENSP00000508581.1:n.301-2A>C
ENST00000507563.7:c.*48-2A>C	ENSP00000510363.1:n.*48-2A>C
ENST00000542946.2:c.*1687A>C	ENSP00000445792.1:n.*1687A>C
ENST00000543594.6:c.*512-2A>C	ENSP00000509354.1:n.*512-2A>C
ENST00000685597.1:c.301-2A>C	ENSP00000509403.1:n.301-2A>C
ENST00000686820.1:c.*48-2A>C	ENSP00000508587.1:n.*48-2A>C
ENST00000688279.1:c.*48-2A>C	ENSP00000510422.1:n.*48-2A>C
ENST00000688430.1:n.227-2A>C
ENST00000689076.1:c.*1687A>C	ENSP00000508469.1:n.*1687A>C
ENST00000689882.1:c.*1752A>C	ENSP00000509351.1:n.*1752A>C
ENST00000691720.1:c.301-2A>C	ENSP00000509146.1:n.301-2A>C
ENST00000692219.1:c.301-2A>C	ENSP00000510149.1:n.301-2A>C
ENST00000692667.1:c.301-2A>C	ENSP00000510180.1:n.301-2A>C
ENST00000692785.1:c.301-2A>C	ENSP00000509310.1:n.301-2A>C
ENST00000693557.1:c.*350A>C	ENSP00000508970.1:n.*350A>C
ENST00000278826.11:c.301-2A>C MANE Select	ENSP00000278826.5:n.301-2A>C
ENST00000278826.10:c.301-2A>C	ENSP00000278826.5:n.301-2A>C
ENST00000381787.2:c.127-2A>C	ENSP00000371206.2:n.127-2A>C
ENST00000423772.6:n.1820-2A>C
ENST00000451389.6:n.442-2A>C
ENST00000507563.6:n.474-2A>C
ENST00000539776.1:n.943A>C
ENST00000542946.1:c.*1687A>C	ENSP00000445792.1:n.*1687A>C
ENST00000543833.1:n.17A>C
ENST00000545420.1:n.325-2A>C
NM_016464.4:c.301-2A>C	NP_057548.1:n.301-2A>C
NR_028473.1:n.743-2A>C
XM_006718585.2:c.301-2A>C	XP_006718648.1:n.301-2A>C
XM_006718586.1:c.301-2A>C	XP_006718649.1:n.301-2A>C
XM_006718588.2:c.127-2A>C	XP_006718651.1:n.127-2A>C
XM_011545098.1:c.301-2A>C	XP_011543400.1:n.301-2A>C
XM_011545099.1:c.301-2A>C	XP_011543401.1:n.301-2A>C
XM_011545100.1:c.301-2A>C	XP_011543402.1:n.301-2A>C
XR_949964.1:n.993A>C
XR_949965.1:n.993A>C
XR_949966.1:n.993A>C
NM_001330281.1:c.127-2A>C	NP_001317210.1:n.127-2A>C
XM_006718585.3:c.301-2A>C	XP_006718648.1:n.301-2A>C
XM_006718586.2:c.301-2A>C	XP_006718649.1:n.301-2A>C
XM_011545098.2:c.301-2A>C	XP_011543400.1:n.301-2A>C
XM_011545099.2:c.301-2A>C	XP_011543401.1:n.301-2A>C
XM_017017917.1:c.300+1705A>C	XP_016873406.1:n.300+1705A>C
XR_949964.3:n.993A>C
XR_949966.2:n.993A>C
NM_016464.5:c.301-2A>C MANE Select	NP_057548.1:n.301-2A>C
NM_001330281.2:c.127-2A>C	NP_001317210.1:n.127-2A>C
NR_028473.2:n.370-2A>C