Canonical Allele Identifier: CA474860151

Gene: SLC22A6

Linked Data

• MyVariant Identifiers: chr11:g.62746968T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62979496T>C , CM000673.2:g.62979496T>C	GRCh38
NC_000011.9:g.62746968T>C , CM000673.1:g.62746968T>C	GRCh37
NC_000011.8:g.62503544T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360421.9:c.1353A>G MANE Select	ENSP00000353597.4:p.Thr451=
ENST00000360421.8:c.1353A>G	ENSP00000353597.4:p.Thr451=
ENST00000377871.7:c.1353A>G	ENSP00000367102.3:p.Thr451=
ENST00000421062.2:c.1353A>G	ENSP00000404441.2:p.Thr451=
ENST00000458333.6:c.1353A>G	ENSP00000396401.2:p.Thr451=
ENST00000540654.5:c.*544A>G	ENSP00000445946.1:n.*544A>G
NM_004790.4:c.1353A>G	NP_004781.2:p.Thr451=
NM_153276.2:c.1353A>G	NP_695008.1:p.Thr451=
NM_153277.2:c.1353A>G	NP_695009.1:p.Thr451=
NM_153278.2:c.1353A>G	NP_695010.1:p.Thr451=
XM_017018562.2:c.1356A>G	XP_016874051.1:p.Thr452=
NM_004790.5:c.1353A>G	NP_004781.2:p.Thr451=
NM_153276.3:c.1353A>G MANE Select	NP_695008.1:p.Thr451=
NM_153277.3:c.1353A>G	NP_695009.1:p.Thr451=
NM_153278.3:c.1353A>G	NP_695010.1:p.Thr451=