Canonical Allele Identifier: CA474860158

Gene: SLC22A6

Linked Data

• MyVariant Identifiers: chr11:g.62746971G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62979499G>A , CM000673.2:g.62979499G>A	GRCh38
NC_000011.9:g.62746971G>A , CM000673.1:g.62746971G>A	GRCh37
NC_000011.8:g.62503547G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360421.9:c.1350C>T MANE Select	ENSP00000353597.4:p.Pro450=
ENST00000360421.8:c.1350C>T	ENSP00000353597.4:p.Pro450=
ENST00000377871.7:c.1350C>T	ENSP00000367102.3:p.Pro450=
ENST00000421062.2:c.1350C>T	ENSP00000404441.2:p.Pro450=
ENST00000458333.6:c.1350C>T	ENSP00000396401.2:p.Pro450=
ENST00000540654.5:c.*541C>T	ENSP00000445946.1:n.*541C>T
NM_004790.4:c.1350C>T	NP_004781.2:p.Pro450=
NM_153276.2:c.1350C>T	NP_695008.1:p.Pro450=
NM_153277.2:c.1350C>T	NP_695009.1:p.Pro450=
NM_153278.2:c.1350C>T	NP_695010.1:p.Pro450=
XM_017018562.2:c.1353C>T	XP_016874051.1:p.Pro451=
NM_004790.5:c.1350C>T	NP_004781.2:p.Pro450=
NM_153276.3:c.1350C>T MANE Select	NP_695008.1:p.Pro450=
NM_153277.3:c.1350C>T	NP_695009.1:p.Pro450=
NM_153278.3:c.1350C>T	NP_695010.1:p.Pro450=