Canonical Allele Identifier: CA912970928

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896438dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025728dup , CM000673.2:g.119025728dup	GRCh38
NC_000011.9:g.118896438dup , CM000673.1:g.118896438dup	GRCh37
NC_000011.8:g.118401648dup	NCBI36
NG_013331.1:g.10180dup , LRG_187:g.10180dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1160dup
ENST00000697845.1:n.2149dup
ENST00000697846.1:n.1160dup
ENST00000697847.1:n.1233dup
ENST00000697848.1:n.1246dup
ENST00000697849.1:n.3264dup
ENST00000697850.1:n.1455dup
ENST00000697851.1:n.2822+241dup
ENST00000638186.1:n.1288+241dup
ENST00000638360.1:n.1120+241dup
ENST00000638925.1:n.1253+241dup
ENST00000650539.1:n.1422dup
ENST00000330775.9:c.984+241dup	ENSP00000476242.2:n.984+241dup
ENST00000357590.9:c.1016dup	ENSP00000476176.2:p.Leu340SerfsTer11
ENST00000524428.5:n.1220+241dup
ENST00000525039.5:n.1440dup
ENST00000525102.5:n.1742+241dup
ENST00000525372.5:n.1082+241dup
ENST00000526275.5:n.1766+241dup
ENST00000527992.5:n.1212+241dup
ENST00000529510.5:n.672+241dup
ENST00000530407.5:n.1134+241dup
ENST00000532085.1:n.4606dup
ENST00000538950.5:c.765+241dup	ENSP00000475991.2:n.765+241dup
ENST00000545985.5:c.984+241dup	ENSP00000475241.2:n.984+241dup
NM_001164277.1:c.984+241dup , LRG_187t1:c.984+241dup	NP_001157749.1:n.984+241dup
NM_001164278.1:c.1016dup	NP_001157750.1:p.Leu340SerfsTer11
NM_001164279.1:c.765+241dup	NP_001157751.1:n.765+241dup
NM_001164280.1:c.984+241dup	NP_001157752.1:n.984+241dup
NM_001467.5:c.984+241dup	NP_001458.1:n.984+241dup
NM_001164278.2:c.1016dup	NP_001157750.1:p.Leu340SerfsTer11
NM_001164279.2:c.765+241dup	NP_001157751.1:n.765+241dup
NM_001164280.2:c.984+241dup	NP_001157752.1:n.984+241dup
NM_001467.6:c.984+241dup	NP_001458.1:n.984+241dup
NM_001164277.2:c.984+241dup MANE Select	NP_001157749.1:n.984+241dup