Canonical Allele Identifier: CA2003750509

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028755_119028756delinsCG , CM000673.2:g.119028755_119028756delinsCG	GRCh38
NC_000011.9:g.118899465_118899466delinsCG , CM000673.1:g.118899465_118899466delinsCG	GRCh37
NC_000011.8:g.118404675_118404676delinsCG	NCBI36
NG_013331.1:g.7151_7152delinsCG , LRG_187:g.7151_7152delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.378-330_378-329delinsCG
ENST00000697846.1:n.378-330_378-329delinsCG
ENST00000697847.1:n.378-330_378-329delinsCG
ENST00000697848.1:n.378-330_378-329delinsCG
ENST00000697849.1:n.1087_1088delinsCG
ENST00000697850.1:n.378-330_378-329delinsCG
ENST00000697851.1:n.1087_1088delinsCG
ENST00000638186.1:n.452-330_452-329delinsCG
ENST00000638360.1:n.386-330_386-329delinsCG
ENST00000638925.1:n.385-330_385-329delinsCG
ENST00000650539.1:n.554-330_554-329delinsCG
ENST00000330775.9:c.149-330_149-329delinsCG	ENSP00000476242.2:n.149-330_149-329delinsCG
ENST00000357590.9:c.149-330_149-329delinsCG	ENSP00000476176.2:n.149-330_149-329delinsCG
ENST00000524428.5:n.149-330_149-329delinsCG
ENST00000525039.5:n.572-330_572-329delinsCG
ENST00000525102.5:n.906-330_906-329delinsCG
ENST00000525372.5:n.149-330_149-329delinsCG
ENST00000525787.1:n.444-330_444-329delinsCG
ENST00000526275.5:n.279_280delinsCG
ENST00000526626.6:n.343+466_343+467delinsCG
ENST00000527992.5:n.376-330_376-329delinsCG
ENST00000529510.5:n.167-330_167-329delinsCG
ENST00000530407.5:n.276_277delinsCG
ENST00000532085.1:n.2108_2109delinsCG
ENST00000532888.6:n.422_423delinsCG
ENST00000534384.1:n.369-330_369-329delinsCG
ENST00000538950.5:c.-93_-92delinsCG	ENSP00000475991.2:n.-93_-92delinsCG
ENST00000545985.5:c.149-330_149-329delinsCG	ENSP00000475241.2:n.149-330_149-329delinsCG
NM_001164277.1:c.149-330_149-329delinsCG , LRG_187t1:c.149-330_149-329delinsCG	NP_001157749.1:n.149-330_149-329delinsCG
NM_001164278.1:c.149-330_149-329delinsCG	NP_001157750.1:n.149-330_149-329delinsCG
NM_001164279.1:c.-93_-92delinsCG	NP_001157751.1:n.-93_-92delinsCG
NM_001164280.1:c.149-330_149-329delinsCG	NP_001157752.1:n.149-330_149-329delinsCG
NM_001467.5:c.149-330_149-329delinsCG	NP_001458.1:n.149-330_149-329delinsCG
NM_001164278.2:c.149-330_149-329delinsCG	NP_001157750.1:n.149-330_149-329delinsCG
NM_001164279.2:c.-93_-92delinsCG	NP_001157751.1:n.-93_-92delinsCG
NM_001164280.2:c.149-330_149-329delinsCG	NP_001157752.1:n.149-330_149-329delinsCG
NM_001467.6:c.149-330_149-329delinsCG	NP_001458.1:n.149-330_149-329delinsCG
NM_001164277.2:c.149-330_149-329delinsCG MANE Select	NP_001157749.1:n.149-330_149-329delinsCG