Canonical Allele Identifier: CA1777308

Gene: TMEM127

Linked Data

• ClinVar Variation Id: 699689
• ClinVar RCV Id: RCV002255555
• dbSNP Id: rs375440877
• ExAC: 2:96919860 G / A
• gnomAD v2: 2-96919860-G-A
• gnomAD v3: 2-96254122-G-A
• gnomAD v4: 2-96254122-G-A
• MyVariant Identifiers: chr2:g.96919860G>A (hg19) ; chr2:g.96254122G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254122G>A , CM000664.2:g.96254122G>A	GRCh38
NC_000002.11:g.96919860G>A , CM000664.1:g.96919860G>A	GRCh37
NC_000002.10:g.96283587G>A	NCBI36
NG_027695.1:g.16892C>T , LRG_528:g.16892C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.410-7C>T MANE Select	ENSP00000258439.3:n.410-7C>T
ENST00000258439.7:c.410-7C>T	ENSP00000258439.2:n.410-7C>T
ENST00000432959.1:c.410-7C>T	ENSP00000416660.1:n.410-7C>T
ENST00000435268.1:c.158-7C>T	ENSP00000411810.1:n.158-7C>T
NM_001193304.2:c.410-7C>T	NP_001180233.1:n.410-7C>T
NM_017849.3:c.410-7C>T , LRG_528t1:c.410-7C>T	NP_060319.1:n.410-7C>T
XM_017004450.1:c.-509-7C>T	XP_016859939.1:n.-509-7C>T
XM_017004452.1:c.158-7C>T	XP_016859941.1:n.158-7C>T
NM_001193304.3:c.410-7C>T	NP_001180233.1:n.410-7C>T
NM_017849.4:c.410-7C>T MANE Select	NP_060319.1:n.410-7C>T