Canonical Allele Identifier: CA2649031512

Gene: SLC19A2

Linked Data

• gnomAD v4: 1-169485530-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169485533dup , CM000663.2:g.169485533dup	GRCh38
NC_000001.10:g.169454771dup , CM000663.1:g.169454771dup	GRCh37
NC_000001.9:g.167721395dup	NCBI36
NG_008255.1:g.5440dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236137.10:c.204+32dup MANE Select	ENSP00000236137.5:n.204+32dup
ENST00000646596.1:c.204+32dup	ENSP00000494404.1:n.204+32dup
ENST00000236137.9:c.204+32dup	ENSP00000236137.5:n.204+32dup
ENST00000367804.4:c.204+32dup	ENSP00000356778.3:n.204+32dup
NM_006996.2:c.204+32dup	NP_008927.1:n.204+32dup
XM_011509076.1:c.12+522dup	XP_011507378.1:n.12+522dup
XM_011509077.1:c.204+32dup	XP_011507379.1:n.204+32dup
NM_001319667.1:c.204+32dup	NP_001306596.1:n.204+32dup
NM_006996.3:c.204+32dup MANE Select	NP_008927.1:n.204+32dup