Canonical Allele Identifier: CA1583124938

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340427_132340431delinsGCTTA , CM000667.2:g.132340427_132340431delinsGCTTA	GRCh38
NC_000005.9:g.131676120_131676124delinsGCTTA , CM000667.1:g.131676120_131676124delinsGCTTA	GRCh37
NC_000005.8:g.131704019_131704023delinsGCTTA	NCBI36
NG_012129.1:g.50976_50980delinsGCTTA
NG_012129.2:g.50976_50980delinsGCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1445-138_1445-134delinsGCTTA (SLC22A4) MANE Select	ENSP00000200652.3:n.1445-138_1445-134delinsGCTTA
ENST00000200652.3:c.1445-138_1445-134delinsGCTTA (SLC22A4)	ENSP00000200652.3:n.1445-138_1445-134delinsGCTTA
NM_003059.2:c.1445-138_1445-134delinsGCTTA (SLC22A4)	NP_003050.2:n.1445-138_1445-134delinsGCTTA
NR_110997.1:n.561-5505_561-5501delinsTAAGC (MIR3936HG)
XM_006714675.2:c.917-138_917-134delinsGCTTA (SLC22A4)	XP_006714738.1:n.917-138_917-134delinsGCTTA
XM_011543589.1:c.1169-138_1169-134delinsGCTTA (SLC22A4)	XP_011541891.1:n.1169-138_1169-134delinsGCTTA
XM_006714675.4:c.917-138_917-134delinsGCTTA (SLC22A4)	XP_006714738.1:n.917-138_917-134delinsGCTTA
XM_011543589.2:c.1169-138_1169-134delinsGCTTA (SLC22A4)	XP_011541891.1:n.1169-138_1169-134delinsGCTTA
XM_017009776.1:c.917-138_917-134delinsGCTTA (SLC22A4)	XP_016865265.1:n.917-138_917-134delinsGCTTA
NM_003059.3:c.1445-138_1445-134delinsGCTTA (SLC22A4) MANE Select	NP_003050.2:n.1445-138_1445-134delinsGCTTA