Canonical Allele Identifier: CA358506125

Gene: TMEM131L

Linked Data

• MyVariant Identifiers: chr4:g.154557522A>G (hg19) ; chr4:g.153636370A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153636370A>G , CM000666.2:g.153636370A>G	GRCh38
NC_000004.11:g.154557522A>G , CM000666.1:g.154557522A>G	GRCh37
NC_000004.10:g.154776972A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409959.8:c.4627A>G MANE Select	ENSP00000386787.3:p.Ser1543Gly
ENST00000240487.5:c.3958A>G	ENSP00000240487.5:p.Ser1320Gly
ENST00000409663.7:c.4624A>G	ENSP00000386574.3:p.Ser1542Gly
ENST00000409959.7:c.4627A>G	ENSP00000386787.3:p.Ser1543Gly
NM_001131007.1:c.4627A>G	NP_001124479.1:p.Ser1543Gly
NM_015196.3:c.4624A>G	NP_056011.3:p.Ser1542Gly
XM_005262871.3:c.2749A>G	XP_005262928.2:p.Ser917Gly
XM_011531780.1:c.4714A>G	XP_011530082.1:p.Ser1572Gly
XM_011531781.1:c.4711A>G	XP_011530083.1:p.Ser1571Gly
XM_011531782.1:c.4684A>G	XP_011530084.1:p.Ser1562Gly
XM_011531783.1:c.4462A>G	XP_011530085.1:p.Ser1488Gly
XM_017007925.1:c.4624A>G	XP_016863414.1:p.Ser1542Gly
XM_017007926.1:c.4621A>G	XP_016863415.1:p.Ser1541Gly
XM_024453956.1:c.4684A>G	XP_024309724.1:p.Ser1562Gly
XM_024453957.1:c.4681A>G	XP_024309725.1:p.Ser1561Gly
XM_024453958.1:c.2749A>G	XP_024309726.1:p.Ser917Gly
NM_001131007.2:c.4627A>G MANE Select	NP_001124479.1:p.Ser1543Gly
NM_015196.4:c.4624A>G	NP_056011.3:p.Ser1542Gly