Canonical Allele Identifier: CA2616340278

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119028833-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028833_119028834insGA , CM000673.2:g.119028833_119028834insGA	GRCh38
NC_000011.9:g.118899543_118899544insGA , CM000673.1:g.118899543_118899544insGA	GRCh37
NC_000011.8:g.118404753_118404754insGA	NCBI36
NG_013331.1:g.7073_7074insTC , LRG_187:g.7073_7074insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.377+388_377+389insTC
ENST00000697846.1:n.377+388_377+389insTC
ENST00000697847.1:n.377+388_377+389insTC
ENST00000697848.1:n.377+388_377+389insTC
ENST00000697849.1:n.1009_1010insTC
ENST00000697850.1:n.377+388_377+389insTC
ENST00000697851.1:n.1009_1010insTC
ENST00000638186.1:n.451+388_451+389insTC
ENST00000638360.1:n.385+388_385+389insTC
ENST00000638925.1:n.384+388_384+389insTC
ENST00000650539.1:n.553+388_553+389insTC
ENST00000330775.9:c.148+388_148+389insTC	ENSP00000476242.2:n.148+388_148+389insTC
ENST00000357590.9:c.148+388_148+389insTC	ENSP00000476176.2:n.148+388_148+389insTC
ENST00000524428.5:n.148+388_148+389insTC
ENST00000525039.5:n.571+388_571+389insTC
ENST00000525102.5:n.905+388_905+389insTC
ENST00000525372.5:n.148+388_148+389insTC
ENST00000525787.1:n.443+388_443+389insTC
ENST00000526275.5:n.201_202insTC
ENST00000526626.6:n.343+388_343+389insTC
ENST00000527992.5:n.375+388_375+389insTC
ENST00000529510.5:n.166+388_166+389insTC
ENST00000530407.5:n.198_199insTC
ENST00000532085.1:n.2030_2031insTC
ENST00000532888.6:n.344_345insTC
ENST00000534384.1:n.368+388_368+389insTC
ENST00000538950.5:c.-171_-170insTC	ENSP00000475991.2:n.-171_-170insTC
ENST00000545985.5:c.148+388_148+389insTC	ENSP00000475241.2:n.148+388_148+389insTC
NM_001164277.1:c.148+388_148+389insTC , LRG_187t1:c.148+388_148+389insTC	NP_001157749.1:n.148+388_148+389insTC
NM_001164278.1:c.148+388_148+389insTC	NP_001157750.1:n.148+388_148+389insTC
NM_001164279.1:c.-171_-170insTC	NP_001157751.1:n.-171_-170insTC
NM_001164280.1:c.148+388_148+389insTC	NP_001157752.1:n.148+388_148+389insTC
NM_001467.5:c.148+388_148+389insTC	NP_001458.1:n.148+388_148+389insTC
NM_001164278.2:c.148+388_148+389insTC	NP_001157750.1:n.148+388_148+389insTC
NM_001164279.2:c.-171_-170insTC	NP_001157751.1:n.-171_-170insTC
NM_001164280.2:c.148+388_148+389insTC	NP_001157752.1:n.148+388_148+389insTC
NM_001467.6:c.148+388_148+389insTC	NP_001458.1:n.148+388_148+389insTC
NM_001164277.2:c.148+388_148+389insTC MANE Select	NP_001157749.1:n.148+388_148+389insTC