Canonical Allele Identifier: CA2616335926

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119027875-G-GCAGGACCTTCCCACA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027875_119027876insCAGGACCTTCCCACA , CM000673.2:g.119027875_119027876insCAGGACCTTCCCACA	GRCh38
NC_000011.9:g.118898585_118898586insCAGGACCTTCCCACA , CM000673.1:g.118898585_118898586insCAGGACCTTCCCACA	GRCh37
NC_000011.8:g.118403795_118403796insCAGGACCTTCCCACA	NCBI36
NG_013331.1:g.8031_8032insTGTGGGAAGGTCCTG , LRG_187:g.8031_8032insTGTGGGAAGGTCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.611-4_611-3insTGTGGGAAGGTCCTG
ENST00000697845.1:n.535-4_535-3insTGTGGGAAGGTCCTG
ENST00000697846.1:n.611-4_611-3insTGTGGGAAGGTCCTG
ENST00000697847.1:n.611-4_611-3insTGTGGGAAGGTCCTG
ENST00000697848.1:n.611-4_611-3insTGTGGGAAGGTCCTG
ENST00000697849.1:n.1650-4_1650-3insTGTGGGAAGGTCCTG
ENST00000697850.1:n.611-4_611-3insTGTGGGAAGGTCCTG
ENST00000697851.1:n.1967_1968insTGTGGGAAGGTCCTG
ENST00000638186.1:n.685-4_685-3insTGTGGGAAGGTCCTG
ENST00000638360.1:n.619-106_619-105insTGTGGGAAGGTCCTG
ENST00000638925.1:n.618-4_618-3insTGTGGGAAGGTCCTG
ENST00000650539.1:n.787-4_787-3insTGTGGGAAGGTCCTG
ENST00000330775.9:c.382-4_382-3insTGTGGGAAGGTCCTG	ENSP00000476242.2:n.382-4_382-3insTGTGGGAAGGTCCTG
ENST00000357590.9:c.382-4_382-3insTGTGGGAAGGTCCTG	ENSP00000476176.2:n.382-4_382-3insTGTGGGAAGGTCCTG
ENST00000524428.5:n.699_700insTGTGGGAAGGTCCTG
ENST00000525039.5:n.805-4_805-3insTGTGGGAAGGTCCTG
ENST00000525102.5:n.1139-4_1139-3insTGTGGGAAGGTCCTG
ENST00000525372.5:n.382-4_382-3insTGTGGGAAGGTCCTG
ENST00000525787.1:n.994_995insTGTGGGAAGGTCCTG
ENST00000526275.5:n.1159_1160insTGTGGGAAGGTCCTG
ENST00000526626.6:n.344-4_344-3insTGTGGGAAGGTCCTG
ENST00000527992.5:n.609-4_609-3insTGTGGGAAGGTCCTG
ENST00000529510.5:n.399+318_399+319insTGTGGGAAGGTCCTG
ENST00000530407.5:n.531-4_531-3insTGTGGGAAGGTCCTG
ENST00000532085.1:n.2988_2989insTGTGGGAAGGTCCTG
ENST00000532888.6:n.677-4_677-3insTGTGGGAAGGTCCTG
ENST00000538950.5:c.163-4_163-3insTGTGGGAAGGTCCTG	ENSP00000475991.2:n.163-4_163-3insTGTGGGAAGGTCCTG
ENST00000545985.5:c.382-4_382-3insTGTGGGAAGGTCCTG	ENSP00000475241.2:n.382-4_382-3insTGTGGGAAGGTCCTG
NM_001164277.1:c.382-4_382-3insTGTGGGAAGGTCCTG , LRG_187t1:c.382-4_382-3insTGTGGGAAGGTCCTG	NP_001157749.1:n.382-4_382-3insTGTGGGAAGGTCCTG
NM_001164278.1:c.382-4_382-3insTGTGGGAAGGTCCTG	NP_001157750.1:n.382-4_382-3insTGTGGGAAGGTCCTG
NM_001164279.1:c.163-4_163-3insTGTGGGAAGGTCCTG	NP_001157751.1:n.163-4_163-3insTGTGGGAAGGTCCTG
NM_001164280.1:c.382-4_382-3insTGTGGGAAGGTCCTG	NP_001157752.1:n.382-4_382-3insTGTGGGAAGGTCCTG
NM_001467.5:c.382-4_382-3insTGTGGGAAGGTCCTG	NP_001458.1:n.382-4_382-3insTGTGGGAAGGTCCTG
NM_001164278.2:c.382-4_382-3insTGTGGGAAGGTCCTG	NP_001157750.1:n.382-4_382-3insTGTGGGAAGGTCCTG
NM_001164279.2:c.163-4_163-3insTGTGGGAAGGTCCTG	NP_001157751.1:n.163-4_163-3insTGTGGGAAGGTCCTG
NM_001164280.2:c.382-4_382-3insTGTGGGAAGGTCCTG	NP_001157752.1:n.382-4_382-3insTGTGGGAAGGTCCTG
NM_001467.6:c.382-4_382-3insTGTGGGAAGGTCCTG	NP_001458.1:n.382-4_382-3insTGTGGGAAGGTCCTG
NM_001164277.2:c.382-4_382-3insTGTGGGAAGGTCCTG MANE Select	NP_001157749.1:n.382-4_382-3insTGTGGGAAGGTCCTG