Canonical Allele Identifier: CA2003749610
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027588_119027589delinsTA , CM000673.2:g.119027588_119027589delinsTA GRCh38
NC_000011.9:g.118898298_118898299delinsTA , CM000673.1:g.118898298_118898299delinsTA GRCh37
NC_000011.8:g.118403508_118403509delinsTA NCBI36
NG_013331.1:g.8317_8318delinsTA , LRG_187:g.8317_8318delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.855+39_855+40delinsTA
ENST00000697845.1:n.779+39_779+40delinsTA
ENST00000697846.1:n.855+39_855+40delinsTA
ENST00000697847.1:n.855+39_855+40delinsTA
ENST00000697848.1:n.855+39_855+40delinsTA
ENST00000697849.1:n.1894+39_1894+40delinsTA
ENST00000697850.1:n.855+39_855+40delinsTA
ENST00000697851.1:n.2215+39_2215+40delinsTA
ENST00000638186.1:n.929+39_929+40delinsTA
ENST00000638360.1:n.761+39_761+40delinsTA
ENST00000638925.1:n.862+39_862+40delinsTA
ENST00000650539.1:n.1031+39_1031+40delinsTA
ENST00000330775.9:c.625+39_625+40delinsTA ENSP00000476242.2:n.625+39_625+40delinsTA...
ENST00000357590.9:c.625+39_625+40delinsTA ENSP00000476176.2:n.625+39_625+40delinsTA...
ENST00000524428.5:n.947+39_947+40delinsTA
ENST00000525039.5:n.1049+39_1049+40delinsTA
ENST00000525102.5:n.1383+39_1383+40delinsTA
ENST00000525372.5:n.626+39_626+40delinsTA
ENST00000526275.5:n.1407+39_1407+40delinsTA
ENST00000526626.6:n.588+39_588+40delinsTA
ENST00000527992.5:n.853+39_853+40delinsTA
ENST00000529510.5:n.400-494_400-493delinsTA
ENST00000530407.5:n.775+39_775+40delinsTA
ENST00000532085.1:n.3236+39_3236+40delinsTA
ENST00000532888.6:n.921+39_921+40delinsTA
ENST00000538950.5:c.406+39_406+40delinsTA ENSP00000475991.2:n.406+39_406+40delinsTA...
ENST00000545985.5:c.625+39_625+40delinsTA ENSP00000475241.2:n.625+39_625+40delinsTA...
NM_001164277.1:c.625+39_625+40delinsTA , LRG_187t1:c.625+39_625+40delinsTA NP_001157749.1:n.625+39_625+40delinsTA
NM_001164278.1:c.625+39_625+40delinsTA NP_001157750.1:n.625+39_625+40delinsTA
NM_001164279.1:c.406+39_406+40delinsTA NP_001157751.1:n.406+39_406+40delinsTA
NM_001164280.1:c.625+39_625+40delinsTA NP_001157752.1:n.625+39_625+40delinsTA
NM_001467.5:c.625+39_625+40delinsTA NP_001458.1:n.625+39_625+40delinsTA
NM_001164278.2:c.625+39_625+40delinsTA NP_001157750.1:n.625+39_625+40delinsTA
NM_001164279.2:c.406+39_406+40delinsTA NP_001157751.1:n.406+39_406+40delinsTA
NM_001164280.2:c.625+39_625+40delinsTA NP_001157752.1:n.625+39_625+40delinsTA
NM_001467.6:c.625+39_625+40delinsTA NP_001458.1:n.625+39_625+40delinsTA
NM_001164277.2:c.625+39_625+40delinsTA MANE Select NP_001157749.1:n.625+39_625+40delinsTA