Canonical Allele Identifier: CA2003749158

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026675_119026677delinsCAT , CM000673.2:g.119026675_119026677delinsCAT	GRCh38
NC_000011.9:g.118897385_118897387delinsCAT , CM000673.1:g.118897385_118897387delinsCAT	GRCh37
NC_000011.8:g.118402595_118402597delinsCAT	NCBI36
NG_013331.1:g.9229_9231delinsATG , LRG_187:g.9229_9231delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+260_1014+262delinsATG
ENST00000697845.1:n.1198_1200delinsATG
ENST00000697846.1:n.1014+260_1014+262delinsATG
ENST00000697847.1:n.1026_1028delinsATG
ENST00000697848.1:n.1026_1028delinsATG
ENST00000697849.1:n.2313_2315delinsATG
ENST00000697850.1:n.1026_1028delinsATG
ENST00000697851.1:n.2634_2636delinsATG
ENST00000638186.1:n.1100_1102delinsATG
ENST00000638360.1:n.932_934delinsATG
ENST00000638925.1:n.1033_1035delinsATG
ENST00000650539.1:n.1202_1204delinsATG
ENST00000330775.9:c.796_798delinsATG	ENSP00000476242.2:p.Met266=
ENST00000357590.9:c.796_798delinsATG	ENSP00000476176.2:p.Met266=
ENST00000524428.5:n.1106+260_1106+262delinsATG
ENST00000525039.5:n.1220_1222delinsATG
ENST00000525102.5:n.1554_1556delinsATG
ENST00000525372.5:n.797_799delinsATG
ENST00000526275.5:n.1578_1580delinsATG
ENST00000527992.5:n.1024_1026delinsATG
ENST00000529510.5:n.558+260_558+262delinsATG
ENST00000530407.5:n.946_948delinsATG
ENST00000532085.1:n.3655_3657delinsATG
ENST00000532888.6:n.1340_1342delinsATG
ENST00000538950.5:c.577_579delinsATG	ENSP00000475991.2:p.Met193=
ENST00000545985.5:c.796_798delinsATG	ENSP00000475241.2:p.Met266=
NM_001164277.1:c.796_798delinsATG , LRG_187t1:c.796_798delinsATG	NP_001157749.1:p.Met266=
NM_001164278.1:c.796_798delinsATG	NP_001157750.1:p.Met266=
NM_001164279.1:c.577_579delinsATG	NP_001157751.1:p.Met193=
NM_001164280.1:c.796_798delinsATG	NP_001157752.1:p.Met266=
NM_001467.5:c.796_798delinsATG	NP_001458.1:p.Met266=
NM_001164278.2:c.796_798delinsATG	NP_001157750.1:p.Met266=
NM_001164279.2:c.577_579delinsATG	NP_001157751.1:p.Met193=
NM_001164280.2:c.796_798delinsATG	NP_001157752.1:p.Met266=
NM_001467.6:c.796_798delinsATG	NP_001458.1:p.Met266=
NM_001164277.2:c.796_798delinsATG MANE Select	NP_001157749.1:p.Met266=