Canonical Allele Identifier: CA474515333
Community Standard Title: NM_016464.5(TMEM138):c.231G>A (p.Lys77=)
Gene: TMEM138 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61366147G>A , CM000673.2:g.61366147G>A GRCh38
NC_000011.9:g.61133619G>A , CM000673.1:g.61133619G>A GRCh37
NC_000011.8:g.60890195G>A NCBI36
NG_032581.1:g.9147G>A

Transcript Alleles

HGVS Amino-acid Change
NM_016464.5:c.231G>A MANE Select NP_057548.1:p.Lys77=
ENST00000278826.11:c.231G>A MANE Select ENSP00000278826.5:p.Lys77=
NM_001330281.1:c.57G>A NP_001317210.1:p.Lys19=
NM_001330281.2:c.57G>A NP_001317210.1:p.Lys19=
NM_016464.4:c.231G>A NP_057548.1:p.Lys77=
NR_028473.1:n.673G>A
NR_028473.2:n.300G>A
ENST00000278826.10:c.231G>A ENSP00000278826.5:p.Lys77=
ENST00000381787.2:c.57G>A ENSP00000371206.2:p.Lys19=
ENST00000423772.6:n.1750G>A
ENST00000451389.6:n.372G>A
ENST00000451389.7:c.231G>A ENSP00000508581.1:p.Lys77=
ENST00000507563.6:n.404G>A
ENST00000507563.7:c.173G>A ENSP00000510363.1:p.Ser58Asn
ENST00000534963.5:n.330G>A
ENST00000540194.5:n.405G>A
ENST00000540194.6:n.990G>A
ENST00000542946.1:c.231G>A ENSP00000445792.1:p.Lys77=
ENST00000542946.2:c.231G>A ENSP00000445792.1:p.Lys77=
ENST00000543594.6:c.*442G>A ENSP00000509354.1:n.*442G>A
ENST00000545420.1:n.255G>A
ENST00000685597.1:c.231G>A ENSP00000509403.1:p.Lys77=
ENST00000686820.1:c.173G>A ENSP00000508587.1:p.Ser58Asn
ENST00000688279.1:c.173G>A ENSP00000510422.1:p.Ser58Asn
ENST00000688430.1:n.157G>A
ENST00000689076.1:c.231G>A ENSP00000508469.1:p.Lys77=
ENST00000689882.1:c.173G>A ENSP00000509351.1:p.Ser58Asn
ENST00000691720.1:c.231G>A ENSP00000509146.1:p.Lys77=
ENST00000692219.1:c.231G>A ENSP00000510149.1:p.Lys77=
ENST00000692667.1:c.231G>A ENSP00000510180.1:p.Lys77=
ENST00000692785.1:c.231G>A ENSP00000509310.1:p.Lys77=
ENST00000693557.1:c.231G>A ENSP00000508970.1:p.Lys77=
XM_006718585.2:c.231G>A XP_006718648.1:p.Lys77=
XM_006718585.3:c.231G>A XP_006718648.1:p.Lys77=
XM_006718586.1:c.231G>A XP_006718649.1:p.Lys77=
XM_006718586.2:c.231G>A XP_006718649.1:p.Lys77=
XM_006718588.2:c.57G>A XP_006718651.1:p.Lys19=
XM_011545098.1:c.231G>A XP_011543400.1:p.Lys77=
XM_011545098.2:c.231G>A XP_011543400.1:p.Lys77=
XM_011545099.1:c.231G>A XP_011543401.1:p.Lys77=
XM_011545099.2:c.231G>A XP_011543401.1:p.Lys77=
XM_011545100.1:c.231G>A XP_011543402.1:p.Lys77=
XM_017017917.1:c.231G>A XP_016873406.1:p.Lys77=
XR_949964.1:n.430G>A
XR_949964.3:n.430G>A
XR_949965.1:n.430G>A
XR_949966.1:n.430G>A
XR_949966.2:n.430G>A