Canonical Allele Identifier: CA2616339515

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024826-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024826G>C , CM000673.2:g.119024826G>C	GRCh38
NC_000011.9:g.118895536G>C , CM000673.1:g.118895536G>C	GRCh37
NC_000011.8:g.118400746G>C	NCBI36
NG_013331.1:g.11080C>G , LRG_187:g.11080C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1584C>G (SLC37A4)
ENST00000697845.1:n.2573C>G (SLC37A4)
ENST00000697846.1:n.1946C>G (SLC37A4)
ENST00000697847.1:n.1657C>G (SLC37A4)
ENST00000697849.1:n.4050C>G (SLC37A4)
ENST00000697850.1:n.2241C>G (SLC37A4)
ENST00000697851.1:n.3212C>G (SLC37A4)
ENST00000638186.1:n.1678C>G (SLC37A4)
ENST00000638360.1:n.1510C>G (SLC37A4)
ENST00000638925.1:n.1643C>G (SLC37A4)
ENST00000650539.1:n.1846C>G (SLC37A4)
ENST00000330775.9:c.*84C>G (SLC37A4)	ENSP00000476242.2:n.*84C>G
ENST00000357590.9:c.*84C>G (SLC37A4)	ENSP00000476176.2:n.*84C>G
ENST00000525102.5:n.2132C>G (SLC37A4)
ENST00000526275.5:n.2156C>G (SLC37A4)
ENST00000527992.5:n.1602C>G (SLC37A4)
ENST00000532085.1:n.5392C>G (SLC37A4)
ENST00000533058.5:c.582-31G>C (TRAPPC4)	ENSP00000432920.1:n.582-31G>C
ENST00000538950.5:c.*84C>G (SLC37A4)	ENSP00000475991.2:n.*84C>G
ENST00000545985.5:c.*84C>G (SLC37A4)	ENSP00000475241.2:n.*84C>G
NM_001164277.1:c.*84C>G , LRG_187t1:c.*84C>G (SLC37A4)	NP_001157749.1:n.*84C>G
NM_001164278.1:c.*84C>G (SLC37A4)	NP_001157750.1:n.*84C>G
NM_001164279.1:c.*84C>G (SLC37A4)	NP_001157751.1:n.*84C>G
NM_001164280.1:c.*84C>G (SLC37A4)	NP_001157752.1:n.*84C>G
NM_001467.5:c.*84C>G (SLC37A4)	NP_001458.1:n.*84C>G
NM_001164278.2:c.*84C>G (SLC37A4)	NP_001157750.1:n.*84C>G
NM_001164279.2:c.*84C>G (SLC37A4)	NP_001157751.1:n.*84C>G
NM_001164280.2:c.*84C>G (SLC37A4)	NP_001157752.1:n.*84C>G
NM_001467.6:c.*84C>G (SLC37A4)	NP_001458.1:n.*84C>G
NM_001164277.2:c.*84C>G (SLC37A4) MANE Select	NP_001157749.1:n.*84C>G