Canonical Allele Identifier: CA382892978

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895611G>C (hg19) ; chr11:g.119024901G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024901G>C , CM000673.2:g.119024901G>C	GRCh38
NC_000011.9:g.118895611G>C , CM000673.1:g.118895611G>C	GRCh37
NC_000011.8:g.118400821G>C	NCBI36
NG_013331.1:g.11005C>G , LRG_187:g.11005C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1509C>G (SLC37A4)
ENST00000697845.1:n.2498C>G (SLC37A4)
ENST00000697846.1:n.1871C>G (SLC37A4)
ENST00000697847.1:n.1582C>G (SLC37A4)
ENST00000697849.1:n.3975C>G (SLC37A4)
ENST00000697850.1:n.2166C>G (SLC37A4)
ENST00000697851.1:n.3137C>G (SLC37A4)
ENST00000638186.1:n.1603C>G (SLC37A4)
ENST00000638360.1:n.1435C>G (SLC37A4)
ENST00000638925.1:n.1568C>G (SLC37A4)
ENST00000650539.1:n.1771C>G (SLC37A4)
ENST00000330775.9:c.*9C>G (SLC37A4)	ENSP00000476242.2:n.*9C>G
ENST00000357590.9:c.*9C>G (SLC37A4)	ENSP00000476176.2:n.*9C>G
ENST00000525102.5:n.2057C>G (SLC37A4)
ENST00000526275.5:n.2081C>G (SLC37A4)
ENST00000527992.5:n.1527C>G (SLC37A4)
ENST00000530407.5:n.1449C>G (SLC37A4)
ENST00000532085.1:n.5317C>G (SLC37A4)
ENST00000533058.5:c.626G>C (TRAPPC4)	ENSP00000432920.1:p.Trp209Ser
ENST00000538950.5:c.*9C>G (SLC37A4)	ENSP00000475991.2:n.*9C>G
ENST00000545985.5:c.*9C>G (SLC37A4)	ENSP00000475241.2:n.*9C>G
NM_001164277.1:c.*9C>G , LRG_187t1:c.*9C>G (SLC37A4)	NP_001157749.1:n.*9C>G
NM_001164278.1:c.*9C>G (SLC37A4)	NP_001157750.1:n.*9C>G
NM_001164279.1:c.*9C>G (SLC37A4)	NP_001157751.1:n.*9C>G
NM_001164280.1:c.*9C>G (SLC37A4)	NP_001157752.1:n.*9C>G
NM_001467.5:c.*9C>G (SLC37A4)	NP_001458.1:n.*9C>G
NM_001164278.2:c.*9C>G (SLC37A4)	NP_001157750.1:n.*9C>G
NM_001164279.2:c.*9C>G (SLC37A4)	NP_001157751.1:n.*9C>G
NM_001164280.2:c.*9C>G (SLC37A4)	NP_001157752.1:n.*9C>G
NM_001467.6:c.*9C>G (SLC37A4)	NP_001458.1:n.*9C>G
NM_001164277.2:c.*9C>G (SLC37A4) MANE Select	NP_001157749.1:n.*9C>G