Canonical Allele Identifier: CA3110584

Gene: TMEM131L

Linked Data

• dbSNP Id: rs375188134
• ExAC: 4:154557518 G / T
• gnomAD v2: 4-154557518-G-T
• gnomAD v4: 4-153636366-G-T
• MyVariant Identifiers: chr4:g.154557518G>T (hg19) ; chr4:g.153636366G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153636366G>T , CM000666.2:g.153636366G>T	GRCh38
NC_000004.11:g.154557518G>T , CM000666.1:g.154557518G>T	GRCh37
NC_000004.10:g.154776968G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409959.8:c.4623G>T MANE Select	ENSP00000386787.3:p.Pro1541=
ENST00000240487.5:c.3954G>T	ENSP00000240487.5:p.Pro1318=
ENST00000409663.7:c.4620G>T	ENSP00000386574.3:p.Pro1540=
ENST00000409959.7:c.4623G>T	ENSP00000386787.3:p.Pro1541=
NM_001131007.1:c.4623G>T	NP_001124479.1:p.Pro1541=
NM_015196.3:c.4620G>T	NP_056011.3:p.Pro1540=
XM_005262871.3:c.2745G>T	XP_005262928.2:p.Pro915=
XM_011531780.1:c.4710G>T	XP_011530082.1:p.Pro1570=
XM_011531781.1:c.4707G>T	XP_011530083.1:p.Pro1569=
XM_011531782.1:c.4680G>T	XP_011530084.1:p.Pro1560=
XM_011531783.1:c.4458G>T	XP_011530085.1:p.Pro1486=
XM_017007925.1:c.4620G>T	XP_016863414.1:p.Pro1540=
XM_017007926.1:c.4617G>T	XP_016863415.1:p.Pro1539=
XM_024453956.1:c.4680G>T	XP_024309724.1:p.Pro1560=
XM_024453957.1:c.4677G>T	XP_024309725.1:p.Pro1559=
XM_024453958.1:c.2745G>T	XP_024309726.1:p.Pro915=
NM_001131007.2:c.4623G>T MANE Select	NP_001124479.1:p.Pro1541=
NM_015196.4:c.4620G>T	NP_056011.3:p.Pro1540=