Canonical Allele Identifier: CA942773686

Gene: SLC37A4

Linked Data

• dbSNP Id: rs2134643347
• gnomAD v3: 11-119029208-G-GGA
• gnomAD v4: 11-119029208-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029208_119029209insGA , CM000673.2:g.119029208_119029209insGA	GRCh38
NC_000011.9:g.118899918_118899919insGA , CM000673.1:g.118899918_118899919insGA	GRCh37
NC_000011.8:g.118405128_118405129insGA	NCBI36
NG_013331.1:g.6698_6699insTC , LRG_187:g.6698_6699insTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.377+13_377+14insTC
ENST00000697846.1:n.377+13_377+14insTC
ENST00000697847.1:n.377+13_377+14insTC
ENST00000697848.1:n.377+13_377+14insTC
ENST00000697849.1:n.634_635insTC
ENST00000697850.1:n.377+13_377+14insTC
ENST00000697851.1:n.634_635insTC
ENST00000638186.1:n.451+13_451+14insTC
ENST00000638360.1:n.385+13_385+14insTC
ENST00000638925.1:n.384+13_384+14insTC
ENST00000650539.1:n.553+13_553+14insTC
ENST00000330775.9:c.148+13_148+14insTC	ENSP00000476242.2:n.148+13_148+14insTC
ENST00000357590.9:c.148+13_148+14insTC	ENSP00000476176.2:n.148+13_148+14insTC
ENST00000524428.5:n.148+13_148+14insTC
ENST00000525039.5:n.571+13_571+14insTC
ENST00000525102.5:n.905+13_905+14insTC
ENST00000525372.5:n.148+13_148+14insTC
ENST00000525787.1:n.443+13_443+14insTC
ENST00000526626.6:n.343+13_343+14insTC
ENST00000527992.5:n.375+13_375+14insTC
ENST00000529510.5:n.166+13_166+14insTC
ENST00000530407.5:n.197+183_197+184insTC
ENST00000532085.1:n.1655_1656insTC
ENST00000532888.6:n.343+13_343+14insTC
ENST00000534384.1:n.368+13_368+14insTC
ENST00000538950.5:c.-172+183_-172+184insTC	ENSP00000475991.2:n.-172+183_-172+184insT...
ENST00000545985.5:c.148+13_148+14insTC	ENSP00000475241.2:n.148+13_148+14insTC
NM_001164277.1:c.148+13_148+14insTC , LRG_187t1:c.148+13_148+14insTC	NP_001157749.1:n.148+13_148+14insTC
NM_001164278.1:c.148+13_148+14insTC	NP_001157750.1:n.148+13_148+14insTC
NM_001164279.1:c.-172+183_-172+184insTC	NP_001157751.1:n.-172+183_-172+184insTC
NM_001164280.1:c.148+13_148+14insTC	NP_001157752.1:n.148+13_148+14insTC
NM_001467.5:c.148+13_148+14insTC	NP_001458.1:n.148+13_148+14insTC
NM_001164278.2:c.148+13_148+14insTC	NP_001157750.1:n.148+13_148+14insTC
NM_001164279.2:c.-172+183_-172+184insTC	NP_001157751.1:n.-172+183_-172+184insTC
NM_001164280.2:c.148+13_148+14insTC	NP_001157752.1:n.148+13_148+14insTC
NM_001467.6:c.148+13_148+14insTC	NP_001458.1:n.148+13_148+14insTC
NM_001164277.2:c.148+13_148+14insTC MANE Select	NP_001157749.1:n.148+13_148+14insTC