Canonical Allele Identifier: CA2003748706

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025804_119025805delinsAG , CM000673.2:g.119025804_119025805delinsAG	GRCh38
NC_000011.9:g.118896514_118896515delinsAG , CM000673.1:g.118896514_118896515delinsAG	GRCh37
NC_000011.8:g.118401724_118401725delinsAG	NCBI36
NG_013331.1:g.10101_10102delinsCT , LRG_187:g.10101_10102delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1129-48_1129-47delinsCT
ENST00000697845.1:n.2070_2071delinsCT
ENST00000697846.1:n.1129-48_1129-47delinsCT
ENST00000697847.1:n.1202-48_1202-47delinsCT
ENST00000697848.1:n.1215-48_1215-47delinsCT
ENST00000697849.1:n.3185_3186delinsCT
ENST00000697850.1:n.1376_1377delinsCT
ENST00000697851.1:n.2822+162_2822+163delinsCT
ENST00000638186.1:n.1288+162_1288+163delinsCT
ENST00000638360.1:n.1120+162_1120+163delinsCT
ENST00000638925.1:n.1253+162_1253+163delinsCT
ENST00000650539.1:n.1391-48_1391-47delinsCT
ENST00000330775.9:c.984+162_984+163delinsCT	ENSP00000476242.2:n.984+162_984+163delinsCT
ENST00000357590.9:c.985-48_985-47delinsCT	ENSP00000476176.2:n.985-48_985-47delinsCT
ENST00000524428.5:n.1220+162_1220+163delinsCT
ENST00000525039.5:n.1409-48_1409-47delinsCT
ENST00000525102.5:n.1742+162_1742+163delinsCT
ENST00000525372.5:n.1082+162_1082+163delinsCT
ENST00000526275.5:n.1766+162_1766+163delinsCT
ENST00000527992.5:n.1212+162_1212+163delinsCT
ENST00000529510.5:n.672+162_672+163delinsCT
ENST00000530407.5:n.1134+162_1134+163delinsCT
ENST00000532085.1:n.4527_4528delinsCT
ENST00000538950.5:c.765+162_765+163delinsCT	ENSP00000475991.2:n.765+162_765+163delinsCT
ENST00000545985.5:c.984+162_984+163delinsCT	ENSP00000475241.2:n.984+162_984+163delinsCT
NM_001164277.1:c.984+162_984+163delinsCT , LRG_187t1:c.984+162_984+163delinsCT	NP_001157749.1:n.984+162_984+163delinsCT
NM_001164278.1:c.985-48_985-47delinsCT	NP_001157750.1:n.985-48_985-47delinsCT
NM_001164279.1:c.765+162_765+163delinsCT	NP_001157751.1:n.765+162_765+163delinsCT
NM_001164280.1:c.984+162_984+163delinsCT	NP_001157752.1:n.984+162_984+163delinsCT
NM_001467.5:c.984+162_984+163delinsCT	NP_001458.1:n.984+162_984+163delinsCT
NM_001164278.2:c.985-48_985-47delinsCT	NP_001157750.1:n.985-48_985-47delinsCT
NM_001164279.2:c.765+162_765+163delinsCT	NP_001157751.1:n.765+162_765+163delinsCT
NM_001164280.2:c.984+162_984+163delinsCT	NP_001157752.1:n.984+162_984+163delinsCT
NM_001467.6:c.984+162_984+163delinsCT	NP_001458.1:n.984+162_984+163delinsCT
NM_001164277.2:c.984+162_984+163delinsCT MANE Select	NP_001157749.1:n.984+162_984+163delinsCT