Canonical Allele Identifier: CA441799807

Gene: TMEM131L

Linked Data

• dbSNP Id: rs2126964213
• gnomAD v4: 4-153636375-T-C
• MyVariant Identifiers: chr4:g.154557527T>C (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000409959.8:c.4632T>C MANE Select	ENSP00000386787.3:p.Asp1544=
ENST00000240487.5:c.3963T>C	ENSP00000240487.5:p.Asp1321=
ENST00000409663.7:c.4629T>C	ENSP00000386574.3:p.Asp1543=
ENST00000409959.7:c.4632T>C	ENSP00000386787.3:p.Asp1544=
NM_001131007.1:c.4632T>C	NP_001124479.1:p.Asp1544=
NM_015196.3:c.4629T>C	NP_056011.3:p.Asp1543=
XM_005262871.3:c.2754T>C	XP_005262928.2:p.Asp918=
XM_011531780.1:c.4719T>C	XP_011530082.1:p.Asp1573=
XM_011531781.1:c.4716T>C	XP_011530083.1:p.Asp1572=
XM_011531782.1:c.4689T>C	XP_011530084.1:p.Asp1563=
XM_011531783.1:c.4467T>C	XP_011530085.1:p.Asp1489=
XM_017007925.1:c.4629T>C	XP_016863414.1:p.Asp1543=
XM_017007926.1:c.4626T>C	XP_016863415.1:p.Asp1542=
XM_024453956.1:c.4689T>C	XP_024309724.1:p.Asp1563=
XM_024453957.1:c.4686T>C	XP_024309725.1:p.Asp1562=
XM_024453958.1:c.2754T>C	XP_024309726.1:p.Asp918=
NM_001131007.2:c.4632T>C MANE Select	NP_001124479.1:p.Asp1544=
NM_015196.4:c.4629T>C	NP_056011.3:p.Asp1543=