Canonical Allele Identifier: CA2616340275

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119028828-G-GTCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028832_119028835dup , CM000673.2:g.119028832_119028835dup	GRCh38
NC_000011.9:g.118899542_118899545dup , CM000673.1:g.118899542_118899545dup	GRCh37
NC_000011.8:g.118404752_118404755dup	NCBI36
NG_013331.1:g.7075_7078dup , LRG_187:g.7075_7078dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.377+390_377+393dup
ENST00000697846.1:n.377+390_377+393dup
ENST00000697847.1:n.377+390_377+393dup
ENST00000697848.1:n.377+390_377+393dup
ENST00000697849.1:n.1011_1014dup
ENST00000697850.1:n.377+390_377+393dup
ENST00000697851.1:n.1011_1014dup
ENST00000638186.1:n.451+390_451+393dup
ENST00000638360.1:n.385+390_385+393dup
ENST00000638925.1:n.384+390_384+393dup
ENST00000650539.1:n.553+390_553+393dup
ENST00000330775.9:c.148+390_148+393dup	ENSP00000476242.2:n.148+390_148+393dup
ENST00000357590.9:c.148+390_148+393dup	ENSP00000476176.2:n.148+390_148+393dup
ENST00000524428.5:n.148+390_148+393dup
ENST00000525039.5:n.571+390_571+393dup
ENST00000525102.5:n.905+390_905+393dup
ENST00000525372.5:n.148+390_148+393dup
ENST00000525787.1:n.443+390_443+393dup
ENST00000526275.5:n.203_206dup
ENST00000526626.6:n.343+390_343+393dup
ENST00000527992.5:n.375+390_375+393dup
ENST00000529510.5:n.166+390_166+393dup
ENST00000530407.5:n.200_203dup
ENST00000532085.1:n.2032_2035dup
ENST00000532888.6:n.346_349dup
ENST00000534384.1:n.368+390_368+393dup
ENST00000538950.5:c.-169_-166dup
ENST00000545985.5:c.148+390_148+393dup	ENSP00000475241.2:n.148+390_148+393dup
NM_001164277.1:c.148+390_148+393dup , LRG_187t1:c.148+390_148+393dup	NP_001157749.1:n.148+390_148+393dup
NM_001164278.1:c.148+390_148+393dup	NP_001157750.1:n.148+390_148+393dup
NM_001164279.1:c.-169_-166dup
NM_001164280.1:c.148+390_148+393dup	NP_001157752.1:n.148+390_148+393dup
NM_001467.5:c.148+390_148+393dup	NP_001458.1:n.148+390_148+393dup
NM_001164278.2:c.148+390_148+393dup	NP_001157750.1:n.148+390_148+393dup
NM_001164279.2:c.-169_-166dup
NM_001164280.2:c.148+390_148+393dup	NP_001157752.1:n.148+390_148+393dup
NM_001467.6:c.148+390_148+393dup	NP_001458.1:n.148+390_148+393dup
NM_001164277.2:c.148+390_148+393dup MANE Select	NP_001157749.1:n.148+390_148+393dup