Canonical Allele Identifier: CA1583137475

Gene: SLC22A5 MIR3936HG

Linked Data

• dbSNP Id: rs1751809543
• gnomAD v4: 5-132369822-CGGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369824_132369826del , CM000667.2:g.132369824_132369826del	GRCh38
NC_000005.9:g.131705516_131705518del , CM000667.1:g.131705516_131705518del	GRCh37
NC_000005.8:g.131733415_131733417del	NCBI36
NG_008982.1:g.5116_5118del
NG_008982.2:g.5121_5123del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435065.7:c.-149_-147del (SLC22A5)	ENSP00000402760.2:n.-149_-147del
ENST00000245407.8:c.-149_-147del (SLC22A5) MANE Select	ENSP00000245407.3:n.-149_-147del
ENST00000245407.7:c.-149_-147del (SLC22A5)	ENSP00000245407.3:n.-149_-147del
NM_001308122.1:c.-149_-147del (SLC22A5)	NP_001295051.1:n.-149_-147del
NM_003060.3:c.-149_-147del (SLC22A5)	NP_003051.1:n.-149_-147del
NR_110997.1:n.73+19_73+21del (MIR3936HG)
XR_427718.1:n.121_123del (SLC22A5)
XR_948290.1:n.121_123del (SLC22A5)
XR_948291.1:n.121_123del (SLC22A5)
XR_001742215.1:n.121_123del (SLC22A5)
XR_001742216.1:n.121_123del (SLC22A5)
XR_427718.2:n.121_123del (SLC22A5)
XR_948290.2:n.121_123del (SLC22A5)
XR_948291.2:n.121_123del (SLC22A5)
NM_003060.4:c.-149_-147del (SLC22A5) MANE Select	NP_003051.1:n.-149_-147del
NM_001308122.2:c.-149_-147del (SLC22A5)	NP_001295051.1:n.-149_-147del