Canonical Allele Identifier: CA1583124924

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340404_132340405delinsTG , CM000667.2:g.132340404_132340405delinsTG	GRCh38
NC_000005.9:g.131676097_131676098delinsTG , CM000667.1:g.131676097_131676098delinsTG	GRCh37
NC_000005.8:g.131703996_131703997delinsTG	NCBI36
NG_012129.1:g.50953_50954delinsTG
NG_012129.2:g.50953_50954delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1445-161_1445-160delinsTG (SLC22A4) MANE Select	ENSP00000200652.3:n.1445-161_1445-160delinsTG
ENST00000200652.3:c.1445-161_1445-160delinsTG (SLC22A4)	ENSP00000200652.3:n.1445-161_1445-160delinsTG
NM_003059.2:c.1445-161_1445-160delinsTG (SLC22A4)	NP_003050.2:n.1445-161_1445-160delinsTG
NR_110997.1:n.561-5479_561-5478delinsCA (MIR3936HG)
XM_006714675.2:c.917-161_917-160delinsTG (SLC22A4)	XP_006714738.1:n.917-161_917-160delinsTG
XM_011543589.1:c.1169-161_1169-160delinsTG (SLC22A4)	XP_011541891.1:n.1169-161_1169-160delinsTG
XM_006714675.4:c.917-161_917-160delinsTG (SLC22A4)	XP_006714738.1:n.917-161_917-160delinsTG
XM_011543589.2:c.1169-161_1169-160delinsTG (SLC22A4)	XP_011541891.1:n.1169-161_1169-160delinsTG
XM_017009776.1:c.917-161_917-160delinsTG (SLC22A4)	XP_016865265.1:n.917-161_917-160delinsTG
NM_003059.3:c.1445-161_1445-160delinsTG (SLC22A4) MANE Select	NP_003050.2:n.1445-161_1445-160delinsTG