Canonical Allele Identifier: CA358506149

Gene: TMEM131L

Linked Data

• gnomAD v4: 4-153636375-T-A
• MyVariant Identifiers: chr4:g.154557527T>A (hg19) ; chr4:g.153636375T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153636375T>A , CM000666.2:g.153636375T>A	GRCh38
NC_000004.11:g.154557527T>A , CM000666.1:g.154557527T>A	GRCh37
NC_000004.10:g.154776977T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409959.8:c.4632T>A MANE Select	ENSP00000386787.3:p.Asp1544Glu
ENST00000240487.5:c.3963T>A	ENSP00000240487.5:p.Asp1321Glu
ENST00000409663.7:c.4629T>A	ENSP00000386574.3:p.Asp1543Glu
ENST00000409959.7:c.4632T>A	ENSP00000386787.3:p.Asp1544Glu
NM_001131007.1:c.4632T>A	NP_001124479.1:p.Asp1544Glu
NM_015196.3:c.4629T>A	NP_056011.3:p.Asp1543Glu
XM_005262871.3:c.2754T>A	XP_005262928.2:p.Asp918Glu
XM_011531780.1:c.4719T>A	XP_011530082.1:p.Asp1573Glu
XM_011531781.1:c.4716T>A	XP_011530083.1:p.Asp1572Glu
XM_011531782.1:c.4689T>A	XP_011530084.1:p.Asp1563Glu
XM_011531783.1:c.4467T>A	XP_011530085.1:p.Asp1489Glu
XM_017007925.1:c.4629T>A	XP_016863414.1:p.Asp1543Glu
XM_017007926.1:c.4626T>A	XP_016863415.1:p.Asp1542Glu
XM_024453956.1:c.4689T>A	XP_024309724.1:p.Asp1563Glu
XM_024453957.1:c.4686T>A	XP_024309725.1:p.Asp1562Glu
XM_024453958.1:c.2754T>A	XP_024309726.1:p.Asp918Glu
NM_001131007.2:c.4632T>A MANE Select	NP_001124479.1:p.Asp1544Glu
NM_015196.4:c.4629T>A	NP_056011.3:p.Asp1543Glu