Canonical Allele Identifier: CA2003748814

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025986_119026006delinsACTGTTACCCGGAAGAGGTAC , CM000673.2:g.119025986_119026006delinsACTGTTACCCGGAAGAGGTAC	GRCh38
NC_000011.9:g.118896696_118896716delinsACTGTTACCCGGAAGAGGTAC , CM000673.1:g.118896696_118896716delinsACTGTTACCCGGAAGAGGTAC	GRCh37
NC_000011.8:g.118401906_118401926delinsACTGTTACCCGGAAGAGGTAC	NCBI36
NG_013331.1:g.9900_9920delinsGTACCTCTTCCGGGTAACAGT , LRG_187:g.9900_9920delinsGTACCTCTTCCGGGTAACAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1089_1109delinsGTACCTCTTCCGGGTAACAGT
ENST00000697845.1:n.1869_1889delinsGTACCTCTTCCGGGTAACAGT
ENST00000697846.1:n.1089_1109delinsGTACCTCTTCCGGGTAACAGT
ENST00000697847.1:n.1202-249_1202-229delinsGTACCTCTTCCGGGTAACAGT
ENST00000697848.1:n.1175_1195delinsGTACCTCTTCCGGGTAACAGT
ENST00000697849.1:n.2984_3004delinsGTACCTCTTCCGGGTAACAGT
ENST00000697850.1:n.1175_1195delinsGTACCTCTTCCGGGTAACAGT
ENST00000697851.1:n.2783_2803delinsGTACCTCTTCCGGGTAACAGT
ENST00000638186.1:n.1249_1269delinsGTACCTCTTCCGGGTAACAGT
ENST00000638360.1:n.1081_1101delinsGTACCTCTTCCGGGTAACAGT
ENST00000638925.1:n.1214_1234delinsGTACCTCTTCCGGGTAACAGT
ENST00000650539.1:n.1351_1371delinsGTACCTCTTCCGGGTAACAGT
ENST00000330775.9:c.945_965delinsGTACCTCTTCCGGGTAACAGT	ENSP00000476242.2:p.Met315=
ENST00000357590.9:c.945_965delinsGTACCTCTTCCGGGTAACAGT	ENSP00000476176.2:p.Met315=
ENST00000524428.5:n.1181_1201delinsGTACCTCTTCCGGGTAACAGT
ENST00000525039.5:n.1369_1389delinsGTACCTCTTCCGGGTAACAGT
ENST00000525102.5:n.1703_1723delinsGTACCTCTTCCGGGTAACAGT
ENST00000525372.5:n.1043_1063delinsGTACCTCTTCCGGGTAACAGT
ENST00000526275.5:n.1727_1747delinsGTACCTCTTCCGGGTAACAGT
ENST00000527992.5:n.1173_1193delinsGTACCTCTTCCGGGTAACAGT
ENST00000529510.5:n.633_653delinsGTACCTCTTCCGGGTAACAGT
ENST00000530407.5:n.1095_1115delinsGTACCTCTTCCGGGTAACAGT
ENST00000532085.1:n.4326_4346delinsGTACCTCTTCCGGGTAACAGT
ENST00000538950.5:c.726_746delinsGTACCTCTTCCGGGTAACAGT	ENSP00000475991.2:p.Met242=
ENST00000545985.5:c.945_965delinsGTACCTCTTCCGGGTAACAGT	ENSP00000475241.2:p.Met315=
NM_001164277.1:c.945_965delinsGTACCTCTTCCGGGTAACAGT , LRG_187t1:c.945_965delinsGTACCTCTTCCGGGTAACAGT	NP_001157749.1:p.Met315=
NM_001164278.1:c.945_965delinsGTACCTCTTCCGGGTAACAGT	NP_001157750.1:p.Met315=
NM_001164279.1:c.726_746delinsGTACCTCTTCCGGGTAACAGT	NP_001157751.1:p.Met242=
NM_001164280.1:c.945_965delinsGTACCTCTTCCGGGTAACAGT	NP_001157752.1:p.Met315=
NM_001467.5:c.945_965delinsGTACCTCTTCCGGGTAACAGT	NP_001458.1:p.Met315=
NM_001164278.2:c.945_965delinsGTACCTCTTCCGGGTAACAGT	NP_001157750.1:p.Met315=
NM_001164279.2:c.726_746delinsGTACCTCTTCCGGGTAACAGT	NP_001157751.1:p.Met242=
NM_001164280.2:c.945_965delinsGTACCTCTTCCGGGTAACAGT	NP_001157752.1:p.Met315=
NM_001467.6:c.945_965delinsGTACCTCTTCCGGGTAACAGT	NP_001458.1:p.Met315=
NM_001164277.2:c.945_965delinsGTACCTCTTCCGGGTAACAGT MANE Select	NP_001157749.1:p.Met315=