Canonical Allele Identifier: CA342643

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721020_131721191del (hg19) ; chr5:g.132385328_132385499del (hg38)
• PubMed: PMID:9826541

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385329_132385500del , CM000667.2:g.132385329_132385500del	GRCh38
NC_000005.9:g.131721021_131721192del , CM000667.1:g.131721021_131721192del	GRCh37
NC_000005.8:g.131748920_131749091del	NCBI36
NG_008982.1:g.20621_20792del
NG_008982.2:g.20626_20797del

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.665+1015_665+1186del	ENSP00000388838.2:n.665+1015_665+1186del
ENST00000435065.7:c.726_896+1del
ENST00000448810.6:c.654_824+1del
ENST00000686757.1:c.673_843+1del
ENST00000687740.1:n.1814_1985del
ENST00000688151.1:n.1846_2016+1del
ENST00000689271.1:c.671+1009_671+1180del	ENSP00000510797.1:n.671+1009_671+1180del
ENST00000690900.1:c.672-47_795+1del
ENST00000692212.1:n.480_650+1del
ENST00000692355.1:c.204+1028_204+1199del
ENST00000692413.1:c.673_843+1del
ENST00000692825.1:c.722_892+1del
ENST00000693308.1:c.667_837+1del
ENST00000693763.1:n.1814_1984+1del
ENST00000245407.8:c.654_824+1del
ENST00000245407.7:c.654_824+1del
ENST00000415928.5:c.423_593+1del
ENST00000435065.6:c.726_896+1del
ENST00000437841.6:c.395_*139+1del
ENST00000461013.5:n.8076_8246+1del
NM_001308122.1:c.726_896+1del
NM_003060.3:c.654_824+1del
XM_011543590.1:c.36_206+1del
XR_427718.1:n.1014_1184+1del
XR_948290.1:n.995_1165+1del
XR_948291.1:n.1008_1178+1del
XM_011543590.2:c.36_206+1del
XM_017009778.2:c.126_296+1del
XR_001742215.1:n.995_1165+1del
XR_001742216.1:n.1014_1184+1del
XR_427718.2:n.1014_1184+1del
XR_948290.2:n.995_1165+1del
XR_948291.2:n.1008_1178+1del
NM_003060.4:c.654_824+1del
NM_001308122.2:c.726_896+1del