Canonical Allele Identifier: CA229597929

Gene: SLC37A4

Linked Data

• dbSNP Id: rs181924297
• gnomAD v2: 11-118897501-C-T
• gnomAD v3: 11-119026791-C-T
• gnomAD v4: 11-119026791-C-T
• MyVariant Identifiers: chr11:g.118897501C>T (hg19) ; chr11:g.119026791C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026791C>T , CM000673.2:g.119026791C>T	GRCh38
NC_000011.9:g.118897501C>T , CM000673.1:g.118897501C>T	GRCh37
NC_000011.8:g.118402711C>T	NCBI36
NG_013331.1:g.9115G>A , LRG_187:g.9115G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+146G>A
ENST00000697845.1:n.1084G>A
ENST00000697846.1:n.1014+146G>A
ENST00000697847.1:n.1015-103G>A
ENST00000697848.1:n.1015-103G>A
ENST00000697849.1:n.2199G>A
ENST00000697850.1:n.1015-103G>A
ENST00000697851.1:n.2520G>A
ENST00000638186.1:n.1089-103G>A
ENST00000638360.1:n.921-103G>A
ENST00000638925.1:n.1022-103G>A
ENST00000650539.1:n.1191-103G>A
ENST00000330775.9:c.785-103G>A	ENSP00000476242.2:n.785-103G>A
ENST00000357590.9:c.785-103G>A	ENSP00000476176.2:n.785-103G>A
ENST00000524428.5:n.1106+146G>A
ENST00000525039.5:n.1209-103G>A
ENST00000525102.5:n.1543-103G>A
ENST00000525372.5:n.786-103G>A
ENST00000526275.5:n.1567-103G>A
ENST00000527992.5:n.1013-103G>A
ENST00000529510.5:n.558+146G>A
ENST00000530407.5:n.935-103G>A
ENST00000532085.1:n.3541G>A
ENST00000532888.6:n.1226G>A
ENST00000538950.5:c.566-103G>A	ENSP00000475991.2:n.566-103G>A
ENST00000545985.5:c.785-103G>A	ENSP00000475241.2:n.785-103G>A
NM_001164277.1:c.785-103G>A , LRG_187t1:c.785-103G>A	NP_001157749.1:n.785-103G>A
NM_001164278.1:c.785-103G>A	NP_001157750.1:n.785-103G>A
NM_001164279.1:c.566-103G>A	NP_001157751.1:n.566-103G>A
NM_001164280.1:c.785-103G>A	NP_001157752.1:n.785-103G>A
NM_001467.5:c.785-103G>A	NP_001458.1:n.785-103G>A
NM_001164278.2:c.785-103G>A	NP_001157750.1:n.785-103G>A
NM_001164279.2:c.566-103G>A	NP_001157751.1:n.566-103G>A
NM_001164280.2:c.785-103G>A	NP_001157752.1:n.785-103G>A
NM_001467.6:c.785-103G>A	NP_001458.1:n.785-103G>A
NM_001164277.2:c.785-103G>A MANE Select	NP_001157749.1:n.785-103G>A