Canonical Allele Identifier: CA427808034

Gene: TMEM127

Linked Data

• dbSNP Id: rs2104284372
• gnomAD v4: 2-96253990-G-A
• MyVariant Identifiers: chr2:g.96919728G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96253990G>A , CM000664.2:g.96253990G>A	GRCh38
NC_000002.11:g.96919728G>A , CM000664.1:g.96919728G>A	GRCh37
NC_000002.10:g.96283455G>A	NCBI36
NG_027695.1:g.17024C>T , LRG_528:g.17024C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.535C>T MANE Select	ENSP00000258439.3:p.Leu179=
ENST00000258439.7:c.535C>T	ENSP00000258439.2:p.Leu179=
ENST00000432959.1:c.535C>T	ENSP00000416660.1:p.Leu179=
ENST00000435268.1:c.283C>T	ENSP00000411810.1:p.Leu95=
NM_001193304.2:c.535C>T	NP_001180233.1:p.Leu179=
NM_017849.3:c.535C>T , LRG_528t1:c.535C>T	NP_060319.1:p.Leu179=
XM_017004450.1:c.-384C>T	XP_016859939.1:n.-384C>T
XM_017004452.1:c.283C>T	XP_016859941.1:p.Leu95=
NM_001193304.3:c.535C>T	NP_001180233.1:p.Leu179=
NM_017849.4:c.535C>T MANE Select	NP_060319.1:p.Leu179=