Canonical Allele Identifier: CA602577625

Gene: SLC37A4 TRAPPC4

Linked Data

• dbSNP Id: rs1565686114
• gnomAD v2: 11-118895864-TGGG-T
• gnomAD v4: 11-119025154-TGGG-T
• MyVariant Identifiers: chr11:g.118895865_118895867del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025157_119025159del , CM000673.2:g.119025157_119025159del	GRCh38
NC_000011.9:g.118895867_118895869del , CM000673.1:g.118895867_118895869del	GRCh37
NC_000011.8:g.118401077_118401079del	NCBI36
NG_013331.1:g.10749_10751del , LRG_187:g.10749_10751del

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1333+34_1333+36del (SLC37A4)
ENST00000697845.1:n.2322+34_2322+36del (SLC37A4)
ENST00000697846.1:n.1695+34_1695+36del (SLC37A4)
ENST00000697847.1:n.1406+34_1406+36del (SLC37A4)
ENST00000697849.1:n.3799+34_3799+36del (SLC37A4)
ENST00000697850.1:n.1990+34_1990+36del (SLC37A4)
ENST00000697851.1:n.2961+34_2961+36del (SLC37A4)
ENST00000638186.1:n.1427+34_1427+36del (SLC37A4)
ENST00000638360.1:n.1259+34_1259+36del (SLC37A4)
ENST00000638925.1:n.1392+34_1392+36del (SLC37A4)
ENST00000650539.1:n.1595+34_1595+36del (SLC37A4)
ENST00000330775.9:c.1123+34_1123+36del (SLC37A4)	ENSP00000476242.2:n.1123+34_1123+36del
ENST00000357590.9:c.1189+34_1189+36del (SLC37A4)	ENSP00000476176.2:n.1189+34_1189+36del
ENST00000524428.5:n.1359+34_1359+36del (SLC37A4)
ENST00000525039.5:n.1613+34_1613+36del (SLC37A4)
ENST00000525102.5:n.1881+34_1881+36del (SLC37A4)
ENST00000525372.5:n.1221+34_1221+36del (SLC37A4)
ENST00000526275.5:n.1905+34_1905+36del (SLC37A4)
ENST00000527992.5:n.1351+34_1351+36del (SLC37A4)
ENST00000529510.5:n.845_847del (SLC37A4)
ENST00000530407.5:n.1273+34_1273+36del (SLC37A4)
ENST00000532085.1:n.5141+34_5141+36del (SLC37A4)
ENST00000533058.5:c.*108_*110del (TRAPPC4)	ENSP00000432920.1:n.*108_*110del
ENST00000538950.5:c.904+34_904+36del (SLC37A4)	ENSP00000475991.2:n.904+34_904+36del
ENST00000545985.5:c.1123+34_1123+36del (SLC37A4)	ENSP00000475241.2:n.1123+34_1123+36del
NM_001164277.1:c.1123+34_1123+36del , LRG_187t1:c.1123+34_1123+36del (SLC37A4)	NP_001157749.1:n.1123+34_1123+36del
NM_001164278.1:c.1189+34_1189+36del (SLC37A4)	NP_001157750.1:n.1189+34_1189+36del
NM_001164279.1:c.904+34_904+36del (SLC37A4)	NP_001157751.1:n.904+34_904+36del
NM_001164280.1:c.1123+34_1123+36del (SLC37A4)	NP_001157752.1:n.1123+34_1123+36del
NM_001467.5:c.1123+34_1123+36del (SLC37A4)	NP_001458.1:n.1123+34_1123+36del
NM_001164278.2:c.1189+34_1189+36del (SLC37A4)	NP_001157750.1:n.1189+34_1189+36del
NM_001164279.2:c.904+34_904+36del (SLC37A4)	NP_001157751.1:n.904+34_904+36del
NM_001164280.2:c.1123+34_1123+36del (SLC37A4)	NP_001157752.1:n.1123+34_1123+36del
NM_001467.6:c.1123+34_1123+36del (SLC37A4)	NP_001458.1:n.1123+34_1123+36del
NM_001164277.2:c.1123+34_1123+36del (SLC37A4) MANE Select	NP_001157749.1:n.1123+34_1123+36del