Canonical Allele Identifier: CA2616340022

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026130-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026131del , CM000673.2:g.119026131del	GRCh38
NC_000011.9:g.118896841del , CM000673.1:g.118896841del	GRCh37
NC_000011.8:g.118402051del	NCBI36
NG_013331.1:g.9775del , LRG_187:g.9775del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1015-51del
ENST00000697845.1:n.1744del
ENST00000697846.1:n.1015-51del
ENST00000697847.1:n.1201+371del
ENST00000697848.1:n.1101-51del
ENST00000697849.1:n.2859del
ENST00000697850.1:n.1101-51del
ENST00000697851.1:n.2709-51del
ENST00000638186.1:n.1175-51del
ENST00000638360.1:n.1007-51del
ENST00000638925.1:n.1140-51del
ENST00000650539.1:n.1277-51del
ENST00000330775.9:c.871-51del	ENSP00000476242.2:n.871-51del
ENST00000357590.9:c.871-51del	ENSP00000476176.2:n.871-51del
ENST00000524428.5:n.1107-51del
ENST00000525039.5:n.1295-51del
ENST00000525102.5:n.1629-51del
ENST00000525372.5:n.969-51del
ENST00000526275.5:n.1653-51del
ENST00000527992.5:n.1099-51del
ENST00000529510.5:n.559-51del
ENST00000530407.5:n.1021-51del
ENST00000532085.1:n.4201del
ENST00000538950.5:c.652-51del	ENSP00000475991.2:n.652-51del
ENST00000545985.5:c.871-51del	ENSP00000475241.2:n.871-51del
NM_001164277.1:c.871-51del , LRG_187t1:c.871-51del	NP_001157749.1:n.871-51del
NM_001164278.1:c.871-51del	NP_001157750.1:n.871-51del
NM_001164279.1:c.652-51del	NP_001157751.1:n.652-51del
NM_001164280.1:c.871-51del	NP_001157752.1:n.871-51del
NM_001467.5:c.871-51del	NP_001458.1:n.871-51del
NM_001164278.2:c.871-51del	NP_001157750.1:n.871-51del
NM_001164279.2:c.652-51del	NP_001157751.1:n.652-51del
NM_001164280.2:c.871-51del	NP_001157752.1:n.871-51del
NM_001467.6:c.871-51del	NP_001458.1:n.871-51del
NM_001164277.2:c.871-51del MANE Select	NP_001157749.1:n.871-51del