Canonical Allele Identifier: CA2616339984

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119025958-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025960del , CM000673.2:g.119025960del	GRCh38
NC_000011.9:g.118896670del , CM000673.1:g.118896670del	GRCh37
NC_000011.8:g.118401880del	NCBI36
NG_013331.1:g.9947del , LRG_187:g.9947del

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1128+8del
ENST00000697845.1:n.1916del
ENST00000697846.1:n.1128+8del
ENST00000697847.1:n.1202-202del
ENST00000697848.1:n.1214+8del
ENST00000697849.1:n.3031del
ENST00000697850.1:n.1222del
ENST00000697851.1:n.2822+8del
ENST00000638186.1:n.1288+8del
ENST00000638360.1:n.1120+8del
ENST00000638925.1:n.1253+8del
ENST00000650539.1:n.1390+8del
ENST00000330775.9:c.984+8del	ENSP00000476242.2:n.984+8del
ENST00000357590.9:c.984+8del	ENSP00000476176.2:n.984+8del
ENST00000524428.5:n.1220+8del
ENST00000525039.5:n.1408+8del
ENST00000525102.5:n.1742+8del
ENST00000525372.5:n.1082+8del
ENST00000526275.5:n.1766+8del
ENST00000527992.5:n.1212+8del
ENST00000529510.5:n.672+8del
ENST00000530407.5:n.1134+8del
ENST00000532085.1:n.4373del
ENST00000538950.5:c.765+8del	ENSP00000475991.2:n.765+8del
ENST00000545985.5:c.984+8del	ENSP00000475241.2:n.984+8del
NM_001164277.1:c.984+8del , LRG_187t1:c.984+8del	NP_001157749.1:n.984+8del
NM_001164278.1:c.984+8del	NP_001157750.1:n.984+8del
NM_001164279.1:c.765+8del	NP_001157751.1:n.765+8del
NM_001164280.1:c.984+8del	NP_001157752.1:n.984+8del
NM_001467.5:c.984+8del	NP_001458.1:n.984+8del
NM_001164278.2:c.984+8del	NP_001157750.1:n.984+8del
NM_001164279.2:c.765+8del	NP_001157751.1:n.765+8del
NM_001164280.2:c.984+8del	NP_001157752.1:n.984+8del
NM_001467.6:c.984+8del	NP_001458.1:n.984+8del
NM_001164277.2:c.984+8del MANE Select	NP_001157749.1:n.984+8del