Canonical Allele Identifier: CA2675191080

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132313595-GTTATACTGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313598_132313607del , CM000667.2:g.132313598_132313607del	GRCh38
NC_000005.9:g.131649291_131649300del , CM000667.1:g.131649291_131649300del	GRCh37
NC_000005.8:g.131677190_131677199del	NCBI36
NG_012129.1:g.24147_24156del
NG_012129.2:g.24147_24156del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.498-16_498-7del (SLC22A4) MANE Select	ENSP00000200652.3:n.498-16_498-7del
ENST00000200652.3:c.498-16_498-7del (SLC22A4)	ENSP00000200652.3:n.498-16_498-7del
ENST00000491257.1:n.302-16_302-7del (SLC22A4)
NM_003059.2:c.498-16_498-7del (SLC22A4)	NP_003050.2:n.498-16_498-7del
NR_110997.1:n.825-1352_825-1343del (MIR3936HG)
XM_006714675.2:c.-31-16_-31-7del (SLC22A4)	XP_006714738.1:n.-31-16_-31-7del
XM_011543589.1:c.394-16_394-7del (SLC22A4)	XP_011541891.1:n.394-16_394-7del
XM_006714675.4:c.-31-16_-31-7del (SLC22A4)	XP_006714738.1:n.-31-16_-31-7del
XM_011543589.2:c.394-16_394-7del (SLC22A4)	XP_011541891.1:n.394-16_394-7del
XM_017009776.1:c.-31-16_-31-7del (SLC22A4)	XP_016865265.1:n.-31-16_-31-7del
NM_003059.3:c.498-16_498-7del (SLC22A4) MANE Select	NP_003050.2:n.498-16_498-7del