Canonical Allele Identifier: CA2003748362

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025149_119025150delinsAC , CM000673.2:g.119025149_119025150delinsAC	GRCh38
NC_000011.9:g.118895859_118895860delinsAC , CM000673.1:g.118895859_118895860delinsAC	GRCh37
NC_000011.8:g.118401069_118401070delinsAC	NCBI36
NG_013331.1:g.10756_10757delinsGT , LRG_187:g.10756_10757delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1333+41_1333+42delinsGT (SLC37A4)
ENST00000697845.1:n.2322+41_2322+42delinsGT (SLC37A4)
ENST00000697846.1:n.1695+41_1695+42delinsGT (SLC37A4)
ENST00000697847.1:n.1406+41_1406+42delinsGT (SLC37A4)
ENST00000697849.1:n.3799+41_3799+42delinsGT (SLC37A4)
ENST00000697850.1:n.1990+41_1990+42delinsGT (SLC37A4)
ENST00000697851.1:n.2961+41_2961+42delinsGT (SLC37A4)
ENST00000638186.1:n.1427+41_1427+42delinsGT (SLC37A4)
ENST00000638360.1:n.1259+41_1259+42delinsGT (SLC37A4)
ENST00000638925.1:n.1392+41_1392+42delinsGT (SLC37A4)
ENST00000650539.1:n.1595+41_1595+42delinsGT (SLC37A4)
ENST00000330775.9:c.1123+41_1123+42delinsGT (SLC37A4)	ENSP00000476242.2:n.1123+41_1123+42delins...
ENST00000357590.9:c.1189+41_1189+42delinsGT (SLC37A4)	ENSP00000476176.2:n.1189+41_1189+42delins...
ENST00000524428.5:n.1359+41_1359+42delinsGT (SLC37A4)
ENST00000525039.5:n.1613+41_1613+42delinsGT (SLC37A4)
ENST00000525102.5:n.1881+41_1881+42delinsGT (SLC37A4)
ENST00000525372.5:n.1221+41_1221+42delinsGT (SLC37A4)
ENST00000526275.5:n.1905+41_1905+42delinsGT (SLC37A4)
ENST00000527992.5:n.1351+41_1351+42delinsGT (SLC37A4)
ENST00000530407.5:n.1273+41_1273+42delinsGT (SLC37A4)
ENST00000532085.1:n.5141+41_5141+42delinsGT (SLC37A4)
ENST00000533058.5:c.*100_*101delinsAC (TRAPPC4)	ENSP00000432920.1:n.*100_*101delinsAC
ENST00000538950.5:c.904+41_904+42delinsGT (SLC37A4)	ENSP00000475991.2:n.904+41_904+42delinsGT...
ENST00000545985.5:c.1123+41_1123+42delinsGT (SLC37A4)	ENSP00000475241.2:n.1123+41_1123+42delins...
NM_001164277.1:c.1123+41_1123+42delinsGT , LRG_187t1:c.1123+41_1123+42delinsGT (SLC37A4)	NP_001157749.1:n.1123+41_1123+42delinsGT
NM_001164278.1:c.1189+41_1189+42delinsGT (SLC37A4)	NP_001157750.1:n.1189+41_1189+42delinsGT
NM_001164279.1:c.904+41_904+42delinsGT (SLC37A4)	NP_001157751.1:n.904+41_904+42delinsGT
NM_001164280.1:c.1123+41_1123+42delinsGT (SLC37A4)	NP_001157752.1:n.1123+41_1123+42delinsGT
NM_001467.5:c.1123+41_1123+42delinsGT (SLC37A4)	NP_001458.1:n.1123+41_1123+42delinsGT
NM_001164278.2:c.1189+41_1189+42delinsGT (SLC37A4)	NP_001157750.1:n.1189+41_1189+42delinsGT
NM_001164279.2:c.904+41_904+42delinsGT (SLC37A4)	NP_001157751.1:n.904+41_904+42delinsGT
NM_001164280.2:c.1123+41_1123+42delinsGT (SLC37A4)	NP_001157752.1:n.1123+41_1123+42delinsGT
NM_001467.6:c.1123+41_1123+42delinsGT (SLC37A4)	NP_001458.1:n.1123+41_1123+42delinsGT
NM_001164277.2:c.1123+41_1123+42delinsGT (SLC37A4) MANE Select	NP_001157749.1:n.1123+41_1123+42delinsGT