Canonical Allele Identifier: CA369654108

Gene: TMEM139 TMEM139-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143285995C>T , CM000669.2:g.143285995C>T	GRCh38
NC_000007.13:g.142983088C>T , CM000669.1:g.142983088C>T	GRCh37
NC_000007.12:g.142693210C>T	NCBI36
NG_029248.1:g.2781C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001282876.2:c.38C>T (TMEM139) MANE Select	NP_001269805.1:p.Pro13Leu
ENST00000359333.8:c.38C>T (TMEM139) MANE Select	ENSP00000352284.3:p.Pro13Leu
NM_001242773.2:c.38C>T (TMEM139)	NP_001229702.1:p.Pro13Leu
NM_001242774.2:c.38C>T (TMEM139)	NP_001229703.1:p.Pro13Leu
NM_001242774.3:c.38C>T (TMEM139)	NP_001229703.1:p.Pro13Leu
NM_001242775.2:c.38C>T (TMEM139)	NP_001229704.1:p.Pro13Leu
NM_001242775.3:c.38C>T (TMEM139)	NP_001229704.1:p.Pro13Leu
NM_001282876.1:c.38C>T (TMEM139)	NP_001269805.1:p.Pro13Leu
NM_001282877.1:c.38C>T (TMEM139)	NP_001269806.1:p.Pro13Leu
NM_153345.3:c.38C>T (TMEM139)	NP_699176.1:p.Pro13Leu
NR_040003.2:n.497-429C>T (TMEM139)
NR_040003.3:n.489-429C>T (TMEM139)
NR_104250.1:n.178-429C>T (TMEM139)
NR_104251.1:n.77-429C>T (TMEM139)
NR_104252.1:n.175-429C>T (TMEM139)
NR_104253.1:n.101-429C>T (TMEM139)
NR_104253.2:n.42-429C>T (TMEM139)
NR_104254.1:n.199-429C>T (TMEM139)
NR_104254.2:n.140-429C>T (TMEM139)
NR_133932.1:n.340G>A (TMEM139-AS1)
ENST00000359333.7:c.38C>T (TMEM139)	ENSP00000352284.3:p.Pro13Leu
ENST00000409102.5:c.38C>T (TMEM139)	ENSP00000386879.1:p.Pro13Leu
ENST00000409244.5:c.38C>T (TMEM139)	ENSP00000386335.1:p.Pro13Leu
ENST00000409541.5:c.38C>T (TMEM139)	ENSP00000387044.1:p.Pro13Leu
ENST00000410004.1:c.38C>T (TMEM139)	ENSP00000386564.1:p.Pro13Leu
ENST00000471161.1:n.100-429C>T (TMEM139)
ENST00000480421.5:n.126-429C>T (TMEM139)
ENST00000482420.1:n.478-429C>T (TMEM139)
ENST00000487419.1:n.29-429C>T (TMEM139)
XR_928069.1:n.208G>A (TMEM139-AS1)
XR_928070.1:n.75G>A (TMEM139-AS1)
XR_928071.1:n.75G>A (TMEM139-AS1)