Canonical Allele Identifier: CA446337737

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726427T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390735T>C , CM000667.2:g.132390735T>C	GRCh38
NC_000005.9:g.131726427T>C , CM000667.1:g.131726427T>C	GRCh37
NC_000005.8:g.131754326T>C	NCBI36
NG_008982.1:g.26027T>C
NG_008982.2:g.26032T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.939T>C	ENSP00000388838.2:p.Pro313=
ENST00000435065.7:c.1170T>C	ENSP00000402760.2:p.Pro390=
ENST00000448810.6:c.1053-41T>C	ENSP00000401860.2:n.1053-41T>C
ENST00000685543.1:n.1239T>C
ENST00000686757.1:c.*262T>C	ENSP00000510721.1:n.*262T>C
ENST00000687740.1:n.3783T>C
ENST00000688151.1:n.2408T>C
ENST00000689271.1:c.945T>C	ENSP00000510797.1:p.Pro315=
ENST00000690900.1:c.*262T>C	ENSP00000510703.1:n.*262T>C
ENST00000692212.1:n.2710T>C
ENST00000692355.1:c.351T>C
ENST00000692413.1:c.1080T>C	ENSP00000509374.1:p.Pro360=
ENST00000692825.1:c.1166T>C	ENSP00000509447.1:n.1166T>C
ENST00000693308.1:c.1146T>C	ENSP00000509770.1:p.Pro382=
ENST00000693763.1:n.2258T>C
ENST00000245407.8:c.1098T>C MANE Select	ENSP00000245407.3:p.Pro366=
ENST00000245407.7:c.1098T>C	ENSP00000245407.3:p.Pro366=
ENST00000435065.6:c.1170T>C	ENSP00000402760.2:p.Pro390=
ENST00000447841.5:c.112-1698T>C
ENST00000448810.5:c.401-41T>C
ENST00000461013.5:n.8520T>C
ENST00000475308.1:n.1776T>C
ENST00000479605.5:n.201T>C
NM_001308122.1:c.1170T>C	NP_001295051.1:p.Pro390=
NM_003060.3:c.1098T>C	NP_003051.1:p.Pro366=
XM_011543590.1:c.480T>C	XP_011541892.1:p.Pro160=
XR_427718.1:n.1458T>C
XR_948290.1:n.1394-1698T>C
XR_948291.1:n.1452T>C
XM_011543590.2:c.480T>C	XP_011541892.1:p.Pro160=
XM_017009778.2:c.570T>C	XP_016865267.1:p.Pro190=
XR_001742215.1:n.1394-41T>C
XR_001742216.1:n.1413-41T>C
XR_427718.2:n.1458T>C
XR_948290.2:n.1394-1698T>C
XR_948291.2:n.1452T>C
NM_003060.4:c.1098T>C MANE Select	NP_003051.1:p.Pro366=
NM_001308122.2:c.1170T>C	NP_001295051.1:p.Pro390=