Canonical Allele Identifier: CA2556893059

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029437-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029440_119029441del , CM000673.2:g.119029440_119029441del	GRCh38
NC_000011.9:g.118900150_118900151del , CM000673.1:g.118900150_118900151del	GRCh37
NC_000011.8:g.118405360_118405361del	NCBI36
NG_013331.1:g.6468_6469del , LRG_187:g.6468_6469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.160_161del
ENST00000697846.1:n.160_161del
ENST00000697847.1:n.160_161del
ENST00000697848.1:n.160_161del
ENST00000697849.1:n.404_405del
ENST00000697850.1:n.160_161del
ENST00000697851.1:n.404_405del
ENST00000638186.1:n.234_235del
ENST00000638360.1:n.168_169del
ENST00000638925.1:n.167_168del
ENST00000650539.1:n.336_337del
ENST00000330775.9:c.-70_-69del	ENSP00000476242.2:n.-70_-69del
ENST00000357590.9:c.-70_-69del	ENSP00000476176.2:n.-70_-69del
ENST00000525039.5:n.354_355del
ENST00000525102.5:n.688_689del
ENST00000525787.1:n.226_227del
ENST00000526626.6:n.126_127del
ENST00000527992.5:n.158_159del
ENST00000530407.5:n.150_151del
ENST00000532085.1:n.1425_1426del
ENST00000532888.6:n.126_127del
ENST00000534384.1:n.151_152del
ENST00000538950.5:c.-219_-218del	ENSP00000475991.2:n.-219_-218del
ENST00000545985.5:c.-70_-69del	ENSP00000475241.2:n.-70_-69del
NM_001164277.1:c.-70_-69del , LRG_187t1:c.-70_-69del	NP_001157749.1:n.-70_-69del
NM_001164278.1:c.-70_-69del	NP_001157750.1:n.-70_-69del
NM_001164279.1:c.-219_-218del	NP_001157751.1:n.-219_-218del
NM_001164280.1:c.-70_-69del	NP_001157752.1:n.-70_-69del
NM_001467.5:c.-70_-69del	NP_001458.1:n.-70_-69del
NM_001164278.2:c.-70_-69del	NP_001157750.1:n.-70_-69del
NM_001164279.2:c.-219_-218del	NP_001157751.1:n.-219_-218del
NM_001164280.2:c.-70_-69del	NP_001157752.1:n.-70_-69del
NM_001467.6:c.-70_-69del	NP_001458.1:n.-70_-69del
NM_001164277.2:c.-70_-69del MANE Select	NP_001157749.1:n.-70_-69del