Canonical Allele Identifier: CA358506159

Gene: TMEM131L

Linked Data

• MyVariant Identifiers: chr4:g.154557529T>A (hg19) ; chr4:g.153636377T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153636377T>A , CM000666.2:g.153636377T>A	GRCh38
NC_000004.11:g.154557529T>A , CM000666.1:g.154557529T>A	GRCh37
NC_000004.10:g.154776979T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409959.8:c.4634T>A MANE Select	ENSP00000386787.3:p.Val1545Glu
ENST00000240487.5:c.3965T>A	ENSP00000240487.5:p.Val1322Glu
ENST00000409663.7:c.4631T>A	ENSP00000386574.3:p.Val1544Glu
ENST00000409959.7:c.4634T>A	ENSP00000386787.3:p.Val1545Glu
NM_001131007.1:c.4634T>A	NP_001124479.1:p.Val1545Glu
NM_015196.3:c.4631T>A	NP_056011.3:p.Val1544Glu
XM_005262871.3:c.2756T>A	XP_005262928.2:p.Val919Glu
XM_011531780.1:c.4721T>A	XP_011530082.1:p.Val1574Glu
XM_011531781.1:c.4718T>A	XP_011530083.1:p.Val1573Glu
XM_011531782.1:c.4691T>A	XP_011530084.1:p.Val1564Glu
XM_011531783.1:c.4469T>A	XP_011530085.1:p.Val1490Glu
XM_017007925.1:c.4631T>A	XP_016863414.1:p.Val1544Glu
XM_017007926.1:c.4628T>A	XP_016863415.1:p.Val1543Glu
XM_024453956.1:c.4691T>A	XP_024309724.1:p.Val1564Glu
XM_024453957.1:c.4688T>A	XP_024309725.1:p.Val1563Glu
XM_024453958.1:c.2756T>A	XP_024309726.1:p.Val919Glu
NM_001131007.2:c.4634T>A MANE Select	NP_001124479.1:p.Val1545Glu
NM_015196.4:c.4631T>A	NP_056011.3:p.Val1544Glu