Canonical Allele Identifier: CA2003774603

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028929_119028930delinsCT , CM000673.2:g.119028929_119028930delinsCT	GRCh38
NC_000011.9:g.118899639_118899640delinsCT , CM000673.1:g.118899639_118899640delinsCT	GRCh37
NC_000011.8:g.118404849_118404850delinsCT	NCBI36
NG_013331.1:g.6977_6978delinsAG , LRG_187:g.6977_6978delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.377+292_377+293delinsAG
ENST00000697846.1:n.377+292_377+293delinsAG
ENST00000697847.1:n.377+292_377+293delinsAG
ENST00000697848.1:n.377+292_377+293delinsAG
ENST00000697849.1:n.913_914delinsAG
ENST00000697850.1:n.377+292_377+293delinsAG
ENST00000697851.1:n.913_914delinsAG
ENST00000638186.1:n.451+292_451+293delinsAG
ENST00000638360.1:n.385+292_385+293delinsAG
ENST00000638925.1:n.384+292_384+293delinsAG
ENST00000650539.1:n.553+292_553+293delinsAG
ENST00000330775.9:c.148+292_148+293delinsAG	ENSP00000476242.2:n.148+292_148+293delinsAG
ENST00000357590.9:c.148+292_148+293delinsAG	ENSP00000476176.2:n.148+292_148+293delinsAG
ENST00000524428.5:n.148+292_148+293delinsAG
ENST00000525039.5:n.571+292_571+293delinsAG
ENST00000525102.5:n.905+292_905+293delinsAG
ENST00000525372.5:n.148+292_148+293delinsAG
ENST00000525787.1:n.443+292_443+293delinsAG
ENST00000526275.5:n.105_106delinsAG
ENST00000526626.6:n.343+292_343+293delinsAG
ENST00000527992.5:n.375+292_375+293delinsAG
ENST00000529510.5:n.166+292_166+293delinsAG
ENST00000530407.5:n.198-96_198-95delinsAG
ENST00000532085.1:n.1934_1935delinsAG
ENST00000532888.6:n.344-96_344-95delinsAG
ENST00000534384.1:n.368+292_368+293delinsAG
ENST00000538950.5:c.-171-96_-171-95delinsAG	ENSP00000475991.2:n.-171-96_-171-95delinsAG
ENST00000545985.5:c.148+292_148+293delinsAG	ENSP00000475241.2:n.148+292_148+293delinsAG
NM_001164277.1:c.148+292_148+293delinsAG , LRG_187t1:c.148+292_148+293delinsAG	NP_001157749.1:n.148+292_148+293delinsAG
NM_001164278.1:c.148+292_148+293delinsAG	NP_001157750.1:n.148+292_148+293delinsAG
NM_001164279.1:c.-171-96_-171-95delinsAG	NP_001157751.1:n.-171-96_-171-95delinsAG
NM_001164280.1:c.148+292_148+293delinsAG	NP_001157752.1:n.148+292_148+293delinsAG
NM_001467.5:c.148+292_148+293delinsAG	NP_001458.1:n.148+292_148+293delinsAG
NM_001164278.2:c.148+292_148+293delinsAG	NP_001157750.1:n.148+292_148+293delinsAG
NM_001164279.2:c.-171-96_-171-95delinsAG	NP_001157751.1:n.-171-96_-171-95delinsAG
NM_001164280.2:c.148+292_148+293delinsAG	NP_001157752.1:n.148+292_148+293delinsAG
NM_001467.6:c.148+292_148+293delinsAG	NP_001458.1:n.148+292_148+293delinsAG
NM_001164277.2:c.148+292_148+293delinsAG MANE Select	NP_001157749.1:n.148+292_148+293delinsAG