Canonical Allele Identifier: CA2578401720

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313826_132313827del , CM000667.2:g.132313826_132313827del	GRCh38
NC_000005.9:g.131649519_131649520del , CM000667.1:g.131649519_131649520del	GRCh37
NC_000005.8:g.131677418_131677419del	NCBI36
NG_012129.1:g.24375_24376del
NG_012129.2:g.24375_24376del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.652+58_652+59del (SLC22A4) MANE Select	ENSP00000200652.3:n.652+58_652+59del
ENST00000200652.3:c.652+58_652+59del (SLC22A4)	ENSP00000200652.3:n.652+58_652+59del
ENST00000491257.1:n.456+58_456+59del (SLC22A4)
NM_003059.2:c.652+58_652+59del (SLC22A4)	NP_003050.2:n.652+58_652+59del
NR_110997.1:n.825-1573_825-1572del (MIR3936HG)
XM_006714675.2:c.124+58_124+59del (SLC22A4)	XP_006714738.1:n.124+58_124+59del
XM_011543589.1:c.548+58_548+59del (SLC22A4)	XP_011541891.1:n.548+58_548+59del
XM_006714675.4:c.124+58_124+59del (SLC22A4)	XP_006714738.1:n.124+58_124+59del
XM_011543589.2:c.548+58_548+59del (SLC22A4)	XP_011541891.1:n.548+58_548+59del
XM_017009776.1:c.124+58_124+59del (SLC22A4)	XP_016865265.1:n.124+58_124+59del
NM_003059.3:c.652+58_652+59del (SLC22A4) MANE Select	NP_003050.2:n.652+58_652+59del