Canonical Allele Identifier: CA477124957

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119025991-T-C
• MyVariant Identifiers: chr11:g.118896701T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025991T>C , CM000673.2:g.119025991T>C	GRCh38
NC_000011.9:g.118896701T>C , CM000673.1:g.118896701T>C	GRCh37
NC_000011.8:g.118401911T>C	NCBI36
NG_013331.1:g.9915A>G , LRG_187:g.9915A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1104A>G
ENST00000697845.1:n.1884A>G
ENST00000697846.1:n.1104A>G
ENST00000697847.1:n.1202-234A>G
ENST00000697848.1:n.1190A>G
ENST00000697849.1:n.2999A>G
ENST00000697850.1:n.1190A>G
ENST00000697851.1:n.2798A>G
ENST00000638186.1:n.1264A>G
ENST00000638360.1:n.1096A>G
ENST00000638925.1:n.1229A>G
ENST00000650539.1:n.1366A>G
ENST00000330775.9:c.960A>G	ENSP00000476242.2:p.Val320=
ENST00000357590.9:c.960A>G	ENSP00000476176.2:p.Val320=
ENST00000524428.5:n.1196A>G
ENST00000525039.5:n.1384A>G
ENST00000525102.5:n.1718A>G
ENST00000525372.5:n.1058A>G
ENST00000526275.5:n.1742A>G
ENST00000527992.5:n.1188A>G
ENST00000529510.5:n.648A>G
ENST00000530407.5:n.1110A>G
ENST00000532085.1:n.4341A>G
ENST00000538950.5:c.741A>G	ENSP00000475991.2:p.Val247=
ENST00000545985.5:c.960A>G	ENSP00000475241.2:p.Val320=
NM_001164277.1:c.960A>G , LRG_187t1:c.960A>G	NP_001157749.1:p.Val320=
NM_001164278.1:c.960A>G	NP_001157750.1:p.Val320=
NM_001164279.1:c.741A>G	NP_001157751.1:p.Val247=
NM_001164280.1:c.960A>G	NP_001157752.1:p.Val320=
NM_001467.5:c.960A>G	NP_001458.1:p.Val320=
NM_001164278.2:c.960A>G	NP_001157750.1:p.Val320=
NM_001164279.2:c.741A>G	NP_001157751.1:p.Val247=
NM_001164280.2:c.960A>G	NP_001157752.1:p.Val320=
NM_001467.6:c.960A>G	NP_001458.1:p.Val320=
NM_001164277.2:c.960A>G MANE Select	NP_001157749.1:p.Val320=