Canonical Allele Identifier: CA942774004

Gene: SLC37A4

Linked Data

• gnomAD v3: 11-119030002-T-TCTCAATACTTAGCACATAATAGATTTAATTGTTTCCTACAGTTGCCC
• gnomAD v4: 11-119030002-T-TCTCAATACTTAGCACATAATAGATTTAATTGTTTCCTACAGTTGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119030005_119030051dup , CM000673.2:g.119030005_119030051dup	GRCh38
NC_000011.9:g.118900715_118900761dup , CM000673.1:g.118900715_118900761dup	GRCh37
NC_000011.8:g.118405925_118405971dup	NCBI36
NG_013331.1:g.5858_5904dup , LRG_187:g.5858_5904dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-485_35-439dup
ENST00000697846.1:n.35-485_35-439dup
ENST00000697847.1:n.35-485_35-439dup
ENST00000697848.1:n.35-485_35-439dup
ENST00000697850.1:n.35-485_35-439dup
ENST00000638360.1:n.43-485_43-439dup
ENST00000638925.1:n.42-485_42-439dup
ENST00000650539.1:n.210+121_210+167dup
ENST00000330775.9:c.-195-485_-195-439dup	ENSP00000476242.2:n.-195-485_-195-439dup
ENST00000357590.9:c.-195-485_-195-439dup	ENSP00000476176.2:n.-195-485_-195-439dup
ENST00000525039.5:n.229-485_229-439dup
ENST00000525102.5:n.562+183_562+229dup
ENST00000527992.5:n.33-485_33-439dup
ENST00000530407.5:n.25-485_25-439dup
ENST00000532085.1:n.815_861dup
ENST00000538950.5:c.-344-485_-344-439dup	ENSP00000475991.2:n.-344-485_-344-439dup
ENST00000545985.5:c.-196+183_-196+229dup	ENSP00000475241.2:n.-196+183_-196+229dup
NM_001164277.1:c.-196+183_-196+229dup , LRG_187t1:c.-196+183_-196+229dup	NP_001157749.1:n.-196+183_-196+229dup
NM_001164278.1:c.-195-485_-195-439dup	NP_001157750.1:n.-195-485_-195-439dup
NM_001164279.1:c.-344-485_-344-439dup	NP_001157751.1:n.-344-485_-344-439dup
NM_001467.5:c.-195-485_-195-439dup	NP_001458.1:n.-195-485_-195-439dup
NM_001164278.2:c.-195-485_-195-439dup	NP_001157750.1:n.-195-485_-195-439dup
NM_001164279.2:c.-344-485_-344-439dup	NP_001157751.1:n.-344-485_-344-439dup
NM_001467.6:c.-195-485_-195-439dup	NP_001458.1:n.-195-485_-195-439dup
NM_001164277.2:c.-196+183_-196+229dup MANE Select	NP_001157749.1:n.-196+183_-196+229dup