Canonical Allele Identifier: CA470000960

Gene: SLC16A9

Linked Data

• MyVariant Identifiers: chr10:g.61414013G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59654255G>A , CM000672.2:g.59654255G>A	GRCh38
NC_000010.10:g.61414013G>A , CM000672.1:g.61414013G>A	GRCh37
NC_000010.9:g.61084019G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395348.8:c.771C>T MANE Select	ENSP00000378757.3:p.Pro257=
ENST00000395347.1:c.771C>T	ENSP00000378756.1:p.Pro257=
ENST00000395348.7:c.771C>T	ENSP00000378757.3:p.Pro257=
NM_194298.2:c.771C>T	NP_919274.1:p.Pro257=
XM_011539488.1:c.771C>T	XP_011537790.1:p.Pro257=
NM_001323977.1:c.510C>T	NP_001310906.1:p.Pro170=
NM_001323978.1:c.510C>T	NP_001310907.1:p.Pro170=
NM_001323979.1:c.510C>T	NP_001310908.1:p.Pro170=
NM_001323980.1:c.510C>T	NP_001310909.1:p.Pro170=
NM_001323981.1:c.771C>T	NP_001310910.1:p.Pro257=
XM_017015883.1:c.771C>T	XP_016871372.1:p.Pro257=
XM_017015884.2:c.771C>T	XP_016871373.1:p.Pro257=
XM_024447878.1:c.771C>T	XP_024303646.1:p.Pro257=
NM_001323978.2:c.510C>T	NP_001310907.1:p.Pro170=
NM_001323979.2:c.510C>T	NP_001310908.1:p.Pro170=
NM_001323980.2:c.510C>T	NP_001310909.1:p.Pro170=
NM_001323981.2:c.771C>T	NP_001310910.1:p.Pro257=
NM_194298.3:c.771C>T MANE Select	NP_919274.1:p.Pro257=