Canonical Allele Identifier: CA2003749131

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026624_119026628delinsCAGGT , CM000673.2:g.119026624_119026628delinsCAGGT	GRCh38
NC_000011.9:g.118897334_118897338delinsCAGGT , CM000673.1:g.118897334_118897338delinsCAGGT	GRCh37
NC_000011.8:g.118402544_118402548delinsCAGGT	NCBI36
NG_013331.1:g.9278_9282delinsACCTG , LRG_187:g.9278_9282delinsACCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+309_1014+313delinsACCTG
ENST00000697845.1:n.1247_1251delinsACCTG
ENST00000697846.1:n.1014+309_1014+313delinsACCTG
ENST00000697847.1:n.1075_1079delinsACCTG
ENST00000697848.1:n.1075_1079delinsACCTG
ENST00000697849.1:n.2362_2366delinsACCTG
ENST00000697850.1:n.1075_1079delinsACCTG
ENST00000697851.1:n.2683_2687delinsACCTG
ENST00000638186.1:n.1149_1153delinsACCTG
ENST00000638360.1:n.981_985delinsACCTG
ENST00000638925.1:n.1082_1086delinsACCTG
ENST00000650539.1:n.1251_1255delinsACCTG
ENST00000330775.9:c.845_849delinsACCTG	ENSP00000476242.2:p.Tyr282=
ENST00000357590.9:c.845_849delinsACCTG	ENSP00000476176.2:p.Tyr282=
ENST00000524428.5:n.1106+309_1106+313delinsACCTG
ENST00000525039.5:n.1269_1273delinsACCTG
ENST00000525102.5:n.1603_1607delinsACCTG
ENST00000525372.5:n.846_850delinsACCTG
ENST00000526275.5:n.1627_1631delinsACCTG
ENST00000527992.5:n.1073_1077delinsACCTG
ENST00000529510.5:n.558+309_558+313delinsACCTG
ENST00000530407.5:n.995_999delinsACCTG
ENST00000532085.1:n.3704_3708delinsACCTG
ENST00000538950.5:c.626_630delinsACCTG	ENSP00000475991.2:p.Tyr209=
ENST00000545985.5:c.845_849delinsACCTG	ENSP00000475241.2:p.Tyr282=
NM_001164277.1:c.845_849delinsACCTG , LRG_187t1:c.845_849delinsACCTG	NP_001157749.1:p.Tyr282=
NM_001164278.1:c.845_849delinsACCTG	NP_001157750.1:p.Tyr282=
NM_001164279.1:c.626_630delinsACCTG	NP_001157751.1:p.Tyr209=
NM_001164280.1:c.845_849delinsACCTG	NP_001157752.1:p.Tyr282=
NM_001467.5:c.845_849delinsACCTG	NP_001458.1:p.Tyr282=
NM_001164278.2:c.845_849delinsACCTG	NP_001157750.1:p.Tyr282=
NM_001164279.2:c.626_630delinsACCTG	NP_001157751.1:p.Tyr209=
NM_001164280.2:c.845_849delinsACCTG	NP_001157752.1:p.Tyr282=
NM_001467.6:c.845_849delinsACCTG	NP_001458.1:p.Tyr282=
NM_001164277.2:c.845_849delinsACCTG MANE Select	NP_001157749.1:p.Tyr282=