Canonical Allele Identifier: CA421719766

Gene: SLC19A2

Linked Data

• dbSNP Id: rs1553213508
• MyVariant Identifiers: chr1:g.169454879del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485641del , CM000663.2:g.169485641del	GRCh38
NC_000001.10:g.169454879del , CM000663.1:g.169454879del	GRCh37
NC_000001.9:g.167721503del	NCBI36
NG_008255.1:g.5330del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.126del MANE Select	ENSP00000236137.5:p.Phe43SerfsTer11
ENST00000646596.1:c.126del	ENSP00000494404.1:p.Phe43SerfsTer11
ENST00000236137.9:c.126del	ENSP00000236137.5:p.Phe43SerfsTer11
ENST00000367804.4:c.126del	ENSP00000356778.3:p.Phe43SerfsTer11
NM_006996.2:c.126del	NP_008927.1:p.Phe43SerfsTer11
XM_011509076.1:c.12+412del	XP_011507378.1:n.12+412del
XM_011509077.1:c.126del	XP_011507379.1:p.Phe43SerfsTer11
NM_001319667.1:c.126del	NP_001306596.1:p.Phe43SerfsTer11
NM_006996.3:c.126del MANE Select	NP_008927.1:p.Phe43SerfsTer11