Canonical Allele Identifier: CA2003749711

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027740_119027744delinsATAGG , CM000673.2:g.119027740_119027744delinsATAGG	GRCh38
NC_000011.9:g.118898450_118898454delinsATAGG , CM000673.1:g.118898450_118898454delinsATAGG	GRCh37
NC_000011.8:g.118403660_118403664delinsATAGG	NCBI36
NG_013331.1:g.8163_8167delinsCCTAT , LRG_187:g.8163_8167delinsCCTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.739_743delinsCCTAT
ENST00000697845.1:n.663_667delinsCCTAT
ENST00000697846.1:n.739_743delinsCCTAT
ENST00000697847.1:n.739_743delinsCCTAT
ENST00000697848.1:n.739_743delinsCCTAT
ENST00000697849.1:n.1778_1782delinsCCTAT
ENST00000697850.1:n.739_743delinsCCTAT
ENST00000697851.1:n.2099_2103delinsCCTAT
ENST00000638186.1:n.813_817delinsCCTAT
ENST00000638360.1:n.645_649delinsCCTAT
ENST00000638925.1:n.746_750delinsCCTAT
ENST00000650539.1:n.915_919delinsCCTAT
ENST00000330775.9:c.510_514delinsCCTAT	ENSP00000476242.2:p.Ala170=
ENST00000357590.9:c.510_514delinsCCTAT	ENSP00000476176.2:p.Ala170=
ENST00000524428.5:n.831_835delinsCCTAT
ENST00000525039.5:n.933_937delinsCCTAT
ENST00000525102.5:n.1267_1271delinsCCTAT
ENST00000525372.5:n.510_514delinsCCTAT
ENST00000526275.5:n.1291_1295delinsCCTAT
ENST00000526626.6:n.472_476delinsCCTAT
ENST00000527992.5:n.737_741delinsCCTAT
ENST00000529510.5:n.399+450_399+454delinsCCTAT
ENST00000530407.5:n.659_663delinsCCTAT
ENST00000532085.1:n.3120_3124delinsCCTAT
ENST00000532888.6:n.805_809delinsCCTAT
ENST00000538950.5:c.291_295delinsCCTAT	ENSP00000475991.2:p.Ala97=
ENST00000545985.5:c.510_514delinsCCTAT	ENSP00000475241.2:p.Ala170=
NM_001164277.1:c.510_514delinsCCTAT , LRG_187t1:c.510_514delinsCCTAT	NP_001157749.1:p.Ala170=
NM_001164278.1:c.510_514delinsCCTAT	NP_001157750.1:p.Ala170=
NM_001164279.1:c.291_295delinsCCTAT	NP_001157751.1:p.Ala97=
NM_001164280.1:c.510_514delinsCCTAT	NP_001157752.1:p.Ala170=
NM_001467.5:c.510_514delinsCCTAT	NP_001458.1:p.Ala170=
NM_001164278.2:c.510_514delinsCCTAT	NP_001157750.1:p.Ala170=
NM_001164279.2:c.291_295delinsCCTAT	NP_001157751.1:p.Ala97=
NM_001164280.2:c.510_514delinsCCTAT	NP_001157752.1:p.Ala170=
NM_001467.6:c.510_514delinsCCTAT	NP_001458.1:p.Ala170=
NM_001164277.2:c.510_514delinsCCTAT MANE Select	NP_001157749.1:p.Ala170=