Canonical Allele Identifier: CA380680029

Gene: TMEM138

Linked Data

• MyVariant Identifiers: chr11:g.61135395A>C (hg19) ; chr11:g.61367923A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61367923A>C , CM000673.2:g.61367923A>C	GRCh38
NC_000011.9:g.61135395A>C , CM000673.1:g.61135395A>C	GRCh37
NC_000011.8:g.60891971A>C	NCBI36
NG_032581.1:g.10923A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000451389.7:c.301A>C	ENSP00000508581.1:p.Asn101His
ENST00000507563.7:c.*48A>C	ENSP00000510363.1:n.*48A>C
ENST00000542946.2:c.*1689A>C	ENSP00000445792.1:n.*1689A>C
ENST00000543594.6:c.*512A>C	ENSP00000509354.1:n.*512A>C
ENST00000685597.1:c.301A>C	ENSP00000509403.1:p.Asn101His
ENST00000686820.1:c.*48A>C	ENSP00000508587.1:n.*48A>C
ENST00000688279.1:c.*48A>C	ENSP00000510422.1:n.*48A>C
ENST00000688430.1:n.227A>C
ENST00000689076.1:c.*1689A>C	ENSP00000508469.1:n.*1689A>C
ENST00000689882.1:c.*1754A>C	ENSP00000509351.1:n.*1754A>C
ENST00000691720.1:c.301A>C	ENSP00000509146.1:p.Asn101His
ENST00000692219.1:c.301A>C	ENSP00000510149.1:p.Asn101His
ENST00000692667.1:c.301A>C	ENSP00000510180.1:p.Asn101His
ENST00000692785.1:c.301A>C	ENSP00000509310.1:p.Asn101His
ENST00000693557.1:c.*352A>C	ENSP00000508970.1:n.*352A>C
ENST00000278826.11:c.301A>C MANE Select	ENSP00000278826.5:p.Asn101His
ENST00000278826.10:c.301A>C	ENSP00000278826.5:p.Asn101His
ENST00000381787.2:c.127A>C	ENSP00000371206.2:p.Asn43His
ENST00000423772.6:n.1820A>C
ENST00000451389.6:n.442A>C
ENST00000507563.6:n.474A>C
ENST00000539776.1:n.945A>C
ENST00000542946.1:c.*1689A>C	ENSP00000445792.1:n.*1689A>C
ENST00000543833.1:n.19A>C
ENST00000545420.1:n.325A>C
NM_016464.4:c.301A>C	NP_057548.1:p.Asn101His
NR_028473.1:n.743A>C
XM_006718585.2:c.301A>C	XP_006718648.1:p.Asn101His
XM_006718586.1:c.301A>C	XP_006718649.1:p.Asn101His
XM_006718588.2:c.127A>C	XP_006718651.1:p.Asn43His
XM_011545098.1:c.301A>C	XP_011543400.1:p.Asn101His
XM_011545099.1:c.301A>C	XP_011543401.1:p.Asn101His
XM_011545100.1:c.301A>C	XP_011543402.1:p.Asn101His
XR_949964.1:n.995A>C
XR_949965.1:n.995A>C
XR_949966.1:n.995A>C
NM_001330281.1:c.127A>C	NP_001317210.1:p.Asn43His
XM_006718585.3:c.301A>C	XP_006718648.1:p.Asn101His
XM_006718586.2:c.301A>C	XP_006718649.1:p.Asn101His
XM_011545098.2:c.301A>C	XP_011543400.1:p.Asn101His
XM_011545099.2:c.301A>C	XP_011543401.1:p.Asn101His
XM_017017917.1:c.300+1707A>C	XP_016873406.1:n.300+1707A>C
XR_949964.3:n.995A>C
XR_949966.2:n.995A>C
NM_016464.5:c.301A>C MANE Select	NP_057548.1:p.Asn101His
NM_001330281.2:c.127A>C	NP_001317210.1:p.Asn43His
NR_028473.2:n.370A>C