Canonical Allele Identifier: CA1504512158

Gene: TMEM131L

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153636376G= , CM000666.2:g.153636376G=	GRCh38
NC_000004.11:g.154557528G= , CM000666.1:g.154557528G=	GRCh37
NC_000004.10:g.154776978G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409959.8:c.4633G= MANE Select	ENSP00000386787.3:p.Val1545=
ENST00000240487.5:c.3964G=	ENSP00000240487.5:p.Val1322=
ENST00000409663.7:c.4630G=	ENSP00000386574.3:p.Val1544=
ENST00000409959.7:c.4633G=	ENSP00000386787.3:p.Val1545=
NM_001131007.1:c.4633G=	NP_001124479.1:p.Val1545=
NM_015196.3:c.4630G=	NP_056011.3:p.Val1544=
XM_005262871.3:c.2755G=	XP_005262928.2:p.Val919=
XM_011531780.1:c.4720G=	XP_011530082.1:p.Val1574=
XM_011531781.1:c.4717G=	XP_011530083.1:p.Val1573=
XM_011531782.1:c.4690G=	XP_011530084.1:p.Val1564=
XM_011531783.1:c.4468G=	XP_011530085.1:p.Val1490=
XM_017007925.1:c.4630G=	XP_016863414.1:p.Val1544=
XM_017007926.1:c.4627G=	XP_016863415.1:p.Val1543=
XM_024453956.1:c.4690G=	XP_024309724.1:p.Val1564=
XM_024453957.1:c.4687G=	XP_024309725.1:p.Val1563=
XM_024453958.1:c.2755G=	XP_024309726.1:p.Val919=
NM_001131007.2:c.4633G= MANE Select	NP_001124479.1:p.Val1545=
NM_015196.4:c.4630G=	NP_056011.3:p.Val1544=