Canonical Allele Identifier: CA2675193189

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132335764-TAAGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132335768_132335771del , CM000667.2:g.132335768_132335771del	GRCh38
NC_000005.9:g.131671461_131671464del , CM000667.1:g.131671461_131671464del	GRCh37
NC_000005.8:g.131699360_131699363del	NCBI36
NG_012129.1:g.46317_46320del
NG_012129.2:g.46317_46320del

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.1262-50_1262-47del (SLC22A4) MANE Select	ENSP00000200652.3:n.1262-50_1262-47del
ENST00000200652.3:c.1262-50_1262-47del (SLC22A4)	ENSP00000200652.3:n.1262-50_1262-47del
NM_003059.2:c.1262-50_1262-47del (SLC22A4)	NP_003050.2:n.1262-50_1262-47del
NR_110997.1:n.561-842_561-839del (MIR3936HG)
XM_006714675.2:c.734-50_734-47del (SLC22A4)	XP_006714738.1:n.734-50_734-47del
XM_011543589.1:c.986-50_986-47del (SLC22A4)	XP_011541891.1:n.986-50_986-47del
XM_006714675.4:c.734-50_734-47del (SLC22A4)	XP_006714738.1:n.734-50_734-47del
XM_011543589.2:c.986-50_986-47del (SLC22A4)	XP_011541891.1:n.986-50_986-47del
XM_017009776.1:c.734-50_734-47del (SLC22A4)	XP_016865265.1:n.734-50_734-47del
NM_003059.3:c.1262-50_1262-47del (SLC22A4) MANE Select	NP_003050.2:n.1262-50_1262-47del