Canonical Allele Identifier: CA1504512155

Gene: TMEM131L

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153636371G= , CM000666.2:g.153636371G=	GRCh38
NC_000004.11:g.154557523G= , CM000666.1:g.154557523G=	GRCh37
NC_000004.10:g.154776973G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409959.8:c.4628G= MANE Select	ENSP00000386787.3:p.Ser1543=
ENST00000240487.5:c.3959G=	ENSP00000240487.5:p.Ser1320=
ENST00000409663.7:c.4625G=	ENSP00000386574.3:p.Ser1542=
ENST00000409959.7:c.4628G=	ENSP00000386787.3:p.Ser1543=
NM_001131007.1:c.4628G=	NP_001124479.1:p.Ser1543=
NM_015196.3:c.4625G=	NP_056011.3:p.Ser1542=
XM_005262871.3:c.2750G=	XP_005262928.2:p.Ser917=
XM_011531780.1:c.4715G=	XP_011530082.1:p.Ser1572=
XM_011531781.1:c.4712G=	XP_011530083.1:p.Ser1571=
XM_011531782.1:c.4685G=	XP_011530084.1:p.Ser1562=
XM_011531783.1:c.4463G=	XP_011530085.1:p.Ser1488=
XM_017007925.1:c.4625G=	XP_016863414.1:p.Ser1542=
XM_017007926.1:c.4622G=	XP_016863415.1:p.Ser1541=
XM_024453956.1:c.4685G=	XP_024309724.1:p.Ser1562=
XM_024453957.1:c.4682G=	XP_024309725.1:p.Ser1561=
XM_024453958.1:c.2750G=	XP_024309726.1:p.Ser917=
NM_001131007.2:c.4628G= MANE Select	NP_001124479.1:p.Ser1543=
NM_015196.4:c.4625G=	NP_056011.3:p.Ser1542=