Canonical Allele Identifier: CA477125848

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897726C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027016C>A , CM000673.2:g.119027016C>A	GRCh38
NC_000011.9:g.118897726C>A , CM000673.1:g.118897726C>A	GRCh37
NC_000011.8:g.118402936C>A	NCBI36
NG_013331.1:g.8890G>T , LRG_187:g.8890G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.935G>T
ENST00000697845.1:n.859G>T
ENST00000697846.1:n.935G>T
ENST00000697847.1:n.935G>T
ENST00000697848.1:n.935G>T
ENST00000697849.1:n.1974G>T
ENST00000697850.1:n.935G>T
ENST00000697851.1:n.2295G>T
ENST00000638186.1:n.1009G>T
ENST00000638360.1:n.841G>T
ENST00000638925.1:n.942G>T
ENST00000650539.1:n.1111G>T
ENST00000330775.9:c.705G>T	ENSP00000476242.2:p.Val235=
ENST00000357590.9:c.705G>T	ENSP00000476176.2:p.Val235=
ENST00000524428.5:n.1027G>T
ENST00000525039.5:n.1129G>T
ENST00000525102.5:n.1463G>T
ENST00000525372.5:n.706G>T
ENST00000526275.5:n.1487G>T
ENST00000526626.6:n.668G>T
ENST00000527992.5:n.933G>T
ENST00000529510.5:n.479G>T
ENST00000530407.5:n.855G>T
ENST00000532085.1:n.3316G>T
ENST00000532888.6:n.1001G>T
ENST00000538950.5:c.486G>T	ENSP00000475991.2:p.Val162=
ENST00000545985.5:c.705G>T	ENSP00000475241.2:p.Val235=
NM_001164277.1:c.705G>T , LRG_187t1:c.705G>T	NP_001157749.1:p.Val235=
NM_001164278.1:c.705G>T	NP_001157750.1:p.Val235=
NM_001164279.1:c.486G>T	NP_001157751.1:p.Val162=
NM_001164280.1:c.705G>T	NP_001157752.1:p.Val235=
NM_001467.5:c.705G>T	NP_001458.1:p.Val235=
NM_001164278.2:c.705G>T	NP_001157750.1:p.Val235=
NM_001164279.2:c.486G>T	NP_001157751.1:p.Val162=
NM_001164280.2:c.705G>T	NP_001157752.1:p.Val235=
NM_001467.6:c.705G>T	NP_001458.1:p.Val235=
NM_001164277.2:c.705G>T MANE Select	NP_001157749.1:p.Val235=