Canonical Allele Identifier: CA2695212788
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025992dup , CM000673.2:g.119025992dup GRCh38
NC_000011.9:g.118896702dup , CM000673.1:g.118896702dup GRCh37
NC_000011.8:g.118401912dup NCBI36
NG_013331.1:g.9914dup , LRG_187:g.9914dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1103dup
ENST00000697845.1:n.1883dup
ENST00000697846.1:n.1103dup
ENST00000697847.1:n.1202-235dup
ENST00000697848.1:n.1189dup
ENST00000697849.1:n.2998dup
ENST00000697850.1:n.1189dup
ENST00000697851.1:n.2797dup
ENST00000638186.1:n.1263dup
ENST00000638360.1:n.1095dup
ENST00000638925.1:n.1228dup
ENST00000650539.1:n.1365dup
ENST00000330775.9:c.959dup ENSP00000476242.2:p.Thr321AsnfsTer5
ENST00000357590.9:c.959dup ENSP00000476176.2:p.Thr321AsnfsTer5
ENST00000524428.5:n.1195dup
ENST00000525039.5:n.1383dup
ENST00000525102.5:n.1717dup
ENST00000525372.5:n.1057dup
ENST00000526275.5:n.1741dup
ENST00000527992.5:n.1187dup
ENST00000529510.5:n.647dup
ENST00000530407.5:n.1109dup
ENST00000532085.1:n.4340dup
ENST00000538950.5:c.740dup ENSP00000475991.2:p.Thr248AsnfsTer5
ENST00000545985.5:c.959dup ENSP00000475241.2:p.Thr321AsnfsTer5
NM_001164277.1:c.959dup , LRG_187t1:c.959dup NP_001157749.1:p.Thr321AsnfsTer5
NM_001164278.1:c.959dup NP_001157750.1:p.Thr321AsnfsTer5
NM_001164279.1:c.740dup NP_001157751.1:p.Thr248AsnfsTer5
NM_001164280.1:c.959dup NP_001157752.1:p.Thr321AsnfsTer5
NM_001467.5:c.959dup NP_001458.1:p.Thr321AsnfsTer5
NM_001164278.2:c.959dup NP_001157750.1:p.Thr321AsnfsTer5
NM_001164279.2:c.740dup NP_001157751.1:p.Thr248AsnfsTer5
NM_001164280.2:c.959dup NP_001157752.1:p.Thr321AsnfsTer5
NM_001467.6:c.959dup NP_001458.1:p.Thr321AsnfsTer5
NM_001164277.2:c.959dup MANE Select NP_001157749.1:p.Thr321AsnfsTer5