Canonical Allele Identifier: CA915947771

Gene: SLC37A4 TRAPPC4

Linked Data

• ClinVar Variation Id: 766132
• ClinVar RCV Id: RCV001444934
• dbSNP Id: rs1592108198
• gnomAD v4: 11-119025085-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025085G>A , CM000673.2:g.119025085G>A	GRCh38
NC_000011.9:g.118895795G>A , CM000673.1:g.118895795G>A	GRCh37
NC_000011.8:g.118401005G>A	NCBI36
NG_013331.1:g.10821C>T , LRG_187:g.10821C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1334-9C>T (SLC37A4)
ENST00000697845.1:n.2323-9C>T (SLC37A4)
ENST00000697846.1:n.1696-9C>T (SLC37A4)
ENST00000697847.1:n.1407-9C>T (SLC37A4)
ENST00000697849.1:n.3800-9C>T (SLC37A4)
ENST00000697850.1:n.1991-9C>T (SLC37A4)
ENST00000697851.1:n.2962-9C>T (SLC37A4)
ENST00000638186.1:n.1428-9C>T (SLC37A4)
ENST00000638360.1:n.1260-9C>T (SLC37A4)
ENST00000638925.1:n.1393-9C>T (SLC37A4)
ENST00000650539.1:n.1596-9C>T (SLC37A4)
ENST00000330775.9:c.1124-9C>T (SLC37A4)	ENSP00000476242.2:n.1124-9C>T
ENST00000357590.9:c.1190-9C>T (SLC37A4)	ENSP00000476176.2:n.1190-9C>T
ENST00000524428.5:n.1360-9C>T (SLC37A4)
ENST00000525039.5:n.1614-9C>T (SLC37A4)
ENST00000525102.5:n.1882-9C>T (SLC37A4)
ENST00000525372.5:n.1222-9C>T (SLC37A4)
ENST00000526275.5:n.1906-9C>T (SLC37A4)
ENST00000527992.5:n.1352-9C>T (SLC37A4)
ENST00000530407.5:n.1274-9C>T (SLC37A4)
ENST00000532085.1:n.5142-9C>T (SLC37A4)
ENST00000533058.5:c.*36G>A (TRAPPC4)	ENSP00000432920.1:n.*36G>A
ENST00000538950.5:c.905-9C>T (SLC37A4)	ENSP00000475991.2:n.905-9C>T
ENST00000545985.5:c.1124-9C>T (SLC37A4)	ENSP00000475241.2:n.1124-9C>T
NM_001164277.1:c.1124-9C>T , LRG_187t1:c.1124-9C>T (SLC37A4)	NP_001157749.1:n.1124-9C>T
NM_001164278.1:c.1190-9C>T (SLC37A4)	NP_001157750.1:n.1190-9C>T
NM_001164279.1:c.905-9C>T (SLC37A4)	NP_001157751.1:n.905-9C>T
NM_001164280.1:c.1124-9C>T (SLC37A4)	NP_001157752.1:n.1124-9C>T
NM_001467.5:c.1124-9C>T (SLC37A4)	NP_001458.1:n.1124-9C>T
NM_001164278.2:c.1190-9C>T (SLC37A4)	NP_001157750.1:n.1190-9C>T
NM_001164279.2:c.905-9C>T (SLC37A4)	NP_001157751.1:n.905-9C>T
NM_001164280.2:c.1124-9C>T (SLC37A4)	NP_001157752.1:n.1124-9C>T
NM_001467.6:c.1124-9C>T (SLC37A4)	NP_001458.1:n.1124-9C>T
NM_001164277.2:c.1124-9C>T (SLC37A4) MANE Select	NP_001157749.1:n.1124-9C>T