Canonical Allele Identifier: CA358506157
Gene: TMEM131L HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000409959.8:c.4633G>A MANE Select ENSP00000386787.3:p.Val1545Met
ENST00000240487.5:c.3964G>A ENSP00000240487.5:p.Val1322Met
ENST00000409663.7:c.4630G>A ENSP00000386574.3:p.Val1544Met
ENST00000409959.7:c.4633G>A ENSP00000386787.3:p.Val1545Met
NM_001131007.1:c.4633G>A NP_001124479.1:p.Val1545Met
NM_015196.3:c.4630G>A NP_056011.3:p.Val1544Met
XM_005262871.3:c.2755G>A XP_005262928.2:p.Val919Met
XM_011531780.1:c.4720G>A XP_011530082.1:p.Val1574Met
XM_011531781.1:c.4717G>A XP_011530083.1:p.Val1573Met
XM_011531782.1:c.4690G>A XP_011530084.1:p.Val1564Met
XM_011531783.1:c.4468G>A XP_011530085.1:p.Val1490Met
XM_017007925.1:c.4630G>A XP_016863414.1:p.Val1544Met
XM_017007926.1:c.4627G>A XP_016863415.1:p.Val1543Met
XM_024453956.1:c.4690G>A XP_024309724.1:p.Val1564Met
XM_024453957.1:c.4687G>A XP_024309725.1:p.Val1563Met
XM_024453958.1:c.2755G>A XP_024309726.1:p.Val919Met
NM_001131007.2:c.4633G>A MANE Select NP_001124479.1:p.Val1545Met
NM_015196.4:c.4630G>A NP_056011.3:p.Val1544Met