Canonical Allele Identifier: CA477367372

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895983G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025273G>C , CM000673.2:g.119025273G>C	GRCh38
NC_000011.9:g.118895983G>C , CM000673.1:g.118895983G>C	GRCh37
NC_000011.8:g.118401193G>C	NCBI36
NG_013331.1:g.10633C>G , LRG_187:g.10633C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1251C>G (SLC37A4)
ENST00000697845.1:n.2240C>G (SLC37A4)
ENST00000697846.1:n.1613C>G (SLC37A4)
ENST00000697847.1:n.1324C>G (SLC37A4)
ENST00000697849.1:n.3717C>G (SLC37A4)
ENST00000697850.1:n.1908C>G (SLC37A4)
ENST00000697851.1:n.2879C>G (SLC37A4)
ENST00000638186.1:n.1345C>G (SLC37A4)
ENST00000638360.1:n.1177C>G (SLC37A4)
ENST00000638925.1:n.1310C>G (SLC37A4)
ENST00000650539.1:n.1513C>G (SLC37A4)
ENST00000330775.9:c.1041C>G (SLC37A4)	ENSP00000476242.2:p.Ala347=
ENST00000357590.9:c.1107C>G (SLC37A4)	ENSP00000476176.2:p.Ala369=
ENST00000524428.5:n.1277C>G (SLC37A4)
ENST00000525039.5:n.1531C>G (SLC37A4)
ENST00000525102.5:n.1799C>G (SLC37A4)
ENST00000525372.5:n.1139C>G (SLC37A4)
ENST00000526275.5:n.1823C>G (SLC37A4)
ENST00000527992.5:n.1269C>G (SLC37A4)
ENST00000529510.5:n.729C>G (SLC37A4)
ENST00000530407.5:n.1191C>G (SLC37A4)
ENST00000532085.1:n.5059C>G (SLC37A4)
ENST00000533058.5:c.*224G>C (TRAPPC4)	ENSP00000432920.1:n.*224G>C
ENST00000538950.5:c.822C>G (SLC37A4)	ENSP00000475991.2:p.Ala274=
ENST00000545985.5:c.1041C>G (SLC37A4)	ENSP00000475241.2:p.Ala347=
NM_001164277.1:c.1041C>G , LRG_187t1:c.1041C>G (SLC37A4)	NP_001157749.1:p.Ala347=
NM_001164278.1:c.1107C>G (SLC37A4)	NP_001157750.1:p.Ala369=
NM_001164279.1:c.822C>G (SLC37A4)	NP_001157751.1:p.Ala274=
NM_001164280.1:c.1041C>G (SLC37A4)	NP_001157752.1:p.Ala347=
NM_001467.5:c.1041C>G (SLC37A4)	NP_001458.1:p.Ala347=
NM_001164278.2:c.1107C>G (SLC37A4)	NP_001157750.1:p.Ala369=
NM_001164279.2:c.822C>G (SLC37A4)	NP_001157751.1:p.Ala274=
NM_001164280.2:c.1041C>G (SLC37A4)	NP_001157752.1:p.Ala347=
NM_001467.6:c.1041C>G (SLC37A4)	NP_001458.1:p.Ala347=
NM_001164277.2:c.1041C>G (SLC37A4) MANE Select	NP_001157749.1:p.Ala347=