Canonical Allele Identifier: CA2003748263

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024958_119024961delinsTAGG , CM000673.2:g.119024958_119024961delinsTAGG	GRCh38
NC_000011.9:g.118895668_118895671delinsTAGG , CM000673.1:g.118895668_118895671delinsTAGG	GRCh37
NC_000011.8:g.118400878_118400881delinsTAGG	NCBI36
NG_013331.1:g.10945_10948delinsCCTA , LRG_187:g.10945_10948delinsCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1449_1452delinsCCTA (SLC37A4)
ENST00000697845.1:n.2438_2441delinsCCTA (SLC37A4)
ENST00000697846.1:n.1811_1814delinsCCTA (SLC37A4)
ENST00000697847.1:n.1522_1525delinsCCTA (SLC37A4)
ENST00000697849.1:n.3915_3918delinsCCTA (SLC37A4)
ENST00000697850.1:n.2106_2109delinsCCTA (SLC37A4)
ENST00000697851.1:n.3077_3080delinsCCTA (SLC37A4)
ENST00000638186.1:n.1543_1546delinsCCTA (SLC37A4)
ENST00000638360.1:n.1375_1378delinsCCTA (SLC37A4)
ENST00000638925.1:n.1508_1511delinsCCTA (SLC37A4)
ENST00000650539.1:n.1711_1714delinsCCTA (SLC37A4)
ENST00000330775.9:c.1239_1242delinsCCTA (SLC37A4)	ENSP00000476242.2:p.Leu413=
ENST00000357590.9:c.1305_1308delinsCCTA (SLC37A4)	ENSP00000476176.2:p.Leu435=
ENST00000524428.5:n.1475_1478delinsCCTA (SLC37A4)
ENST00000525039.5:n.1729_1732delinsCCTA (SLC37A4)
ENST00000525102.5:n.1997_2000delinsCCTA (SLC37A4)
ENST00000525372.5:n.1337_1340delinsCCTA (SLC37A4)
ENST00000526275.5:n.2021_2024delinsCCTA (SLC37A4)
ENST00000527992.5:n.1467_1470delinsCCTA (SLC37A4)
ENST00000530407.5:n.1389_1392delinsCCTA (SLC37A4)
ENST00000532085.1:n.5257_5260delinsCCTA (SLC37A4)
ENST00000533058.5:c.683_686delinsTAGG (TRAPPC4)	ENSP00000432920.1:p.Val228=
ENST00000538950.5:c.1020_1023delinsCCTA (SLC37A4)	ENSP00000475991.2:p.Leu340=
ENST00000545985.5:c.1239_1242delinsCCTA (SLC37A4)	ENSP00000475241.2:p.Leu413=
NM_001164277.1:c.1239_1242delinsCCTA , LRG_187t1:c.1239_1242delinsCCTA (SLC37A4)	NP_001157749.1:p.Leu413=
NM_001164278.1:c.1305_1308delinsCCTA (SLC37A4)	NP_001157750.1:p.Leu435=
NM_001164279.1:c.1020_1023delinsCCTA (SLC37A4)	NP_001157751.1:p.Leu340=
NM_001164280.1:c.1239_1242delinsCCTA (SLC37A4)	NP_001157752.1:p.Leu413=
NM_001467.5:c.1239_1242delinsCCTA (SLC37A4)	NP_001458.1:p.Leu413=
NM_001164278.2:c.1305_1308delinsCCTA (SLC37A4)	NP_001157750.1:p.Leu435=
NM_001164279.2:c.1020_1023delinsCCTA (SLC37A4)	NP_001157751.1:p.Leu340=
NM_001164280.2:c.1239_1242delinsCCTA (SLC37A4)	NP_001157752.1:p.Leu413=
NM_001467.6:c.1239_1242delinsCCTA (SLC37A4)	NP_001458.1:p.Leu413=
NM_001164277.2:c.1239_1242delinsCCTA (SLC37A4) MANE Select	NP_001157749.1:p.Leu413=