Canonical Allele Identifier: CA912970968

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896798dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026088dup , CM000673.2:g.119026088dup	GRCh38
NC_000011.9:g.118896798dup , CM000673.1:g.118896798dup	GRCh37
NC_000011.8:g.118402008dup	NCBI36
NG_013331.1:g.9818dup , LRG_187:g.9818dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1015-8dup
ENST00000697845.1:n.1787dup
ENST00000697846.1:n.1015-8dup
ENST00000697847.1:n.1202-331dup
ENST00000697848.1:n.1101-8dup
ENST00000697849.1:n.2902dup
ENST00000697850.1:n.1101-8dup
ENST00000697851.1:n.2709-8dup
ENST00000638186.1:n.1175-8dup
ENST00000638360.1:n.1007-8dup
ENST00000638925.1:n.1140-8dup
ENST00000650539.1:n.1277-8dup
ENST00000330775.9:c.871-8dup	ENSP00000476242.2:n.871-8dup
ENST00000357590.9:c.871-8dup	ENSP00000476176.2:n.871-8dup
ENST00000524428.5:n.1107-8dup
ENST00000525039.5:n.1295-8dup
ENST00000525102.5:n.1629-8dup
ENST00000525372.5:n.969-8dup
ENST00000526275.5:n.1653-8dup
ENST00000527992.5:n.1099-8dup
ENST00000529510.5:n.559-8dup
ENST00000530407.5:n.1021-8dup
ENST00000532085.1:n.4244dup
ENST00000538950.5:c.652-8dup	ENSP00000475991.2:n.652-8dup
ENST00000545985.5:c.871-8dup	ENSP00000475241.2:n.871-8dup
NM_001164277.1:c.871-8dup , LRG_187t1:c.871-8dup	NP_001157749.1:n.871-8dup
NM_001164278.1:c.871-8dup	NP_001157750.1:n.871-8dup
NM_001164279.1:c.652-8dup	NP_001157751.1:n.652-8dup
NM_001164280.1:c.871-8dup	NP_001157752.1:n.871-8dup
NM_001467.5:c.871-8dup	NP_001458.1:n.871-8dup
NM_001164278.2:c.871-8dup	NP_001157750.1:n.871-8dup
NM_001164279.2:c.652-8dup	NP_001157751.1:n.652-8dup
NM_001164280.2:c.871-8dup	NP_001157752.1:n.871-8dup
NM_001467.6:c.871-8dup	NP_001458.1:n.871-8dup
NM_001164277.2:c.871-8dup MANE Select	NP_001157749.1:n.871-8dup