Canonical Allele Identifier: CA10639442

Gene: TMEM138

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61362321C>T , CM000673.2:g.61362321C>T	GRCh38
NC_000011.9:g.61129793C>T , CM000673.1:g.61129793C>T	GRCh37
NC_000011.8:g.60886369C>T	NCBI36
NG_032581.1:g.5321C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001330281.1:c.-210C>T	NP_001317210.1:n.-210C>T
NM_016464.4:c.-239C>T	NP_057548.1:n.-239C>T
NR_028473.1:n.321C>T
ENST00000278826.10:c.-239C>T	ENSP00000278826.5:n.-239C>T
ENST00000451389.7:c.-239C>T	ENSP00000508581.1:n.-239C>T
ENST00000540194.6:n.169C>T
ENST00000542946.2:c.-239C>T	ENSP00000445792.1:n.-239C>T
ENST00000685597.1:c.-239C>T	ENSP00000509403.1:n.-239C>T
ENST00000689076.1:c.-239C>T	ENSP00000508469.1:n.-239C>T
ENST00000692667.1:c.-239C>T	ENSP00000510180.1:n.-239C>T
ENST00000692785.1:c.-239C>T	ENSP00000509310.1:n.-239C>T
ENST00000693557.1:c.-239C>T	ENSP00000508970.1:n.-239C>T
XM_006718588.2:c.-210C>T	XP_006718651.1:n.-210C>T