Canonical Allele Identifier: CA2616339895

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119025797-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025797_119025798insGA , CM000673.2:g.119025797_119025798insGA	GRCh38
NC_000011.9:g.118896507_118896508insGA , CM000673.1:g.118896507_118896508insGA	GRCh37
NC_000011.8:g.118401717_118401718insGA	NCBI36
NG_013331.1:g.10108_10109insTC , LRG_187:g.10108_10109insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1129-41_1129-40insTC
ENST00000697845.1:n.2077_2078insTC
ENST00000697846.1:n.1129-41_1129-40insTC
ENST00000697847.1:n.1202-41_1202-40insTC
ENST00000697848.1:n.1215-41_1215-40insTC
ENST00000697849.1:n.3192_3193insTC
ENST00000697850.1:n.1383_1384insTC
ENST00000697851.1:n.2822+169_2822+170insTC
ENST00000638186.1:n.1288+169_1288+170insTC
ENST00000638360.1:n.1120+169_1120+170insTC
ENST00000638925.1:n.1253+169_1253+170insTC
ENST00000650539.1:n.1391-41_1391-40insTC
ENST00000330775.9:c.984+169_984+170insTC	ENSP00000476242.2:n.984+169_984+170insTC
ENST00000357590.9:c.985-41_985-40insTC	ENSP00000476176.2:n.985-41_985-40insTC
ENST00000524428.5:n.1220+169_1220+170insTC
ENST00000525039.5:n.1409-41_1409-40insTC
ENST00000525102.5:n.1742+169_1742+170insTC
ENST00000525372.5:n.1082+169_1082+170insTC
ENST00000526275.5:n.1766+169_1766+170insTC
ENST00000527992.5:n.1212+169_1212+170insTC
ENST00000529510.5:n.672+169_672+170insTC
ENST00000530407.5:n.1134+169_1134+170insTC
ENST00000532085.1:n.4534_4535insTC
ENST00000538950.5:c.765+169_765+170insTC	ENSP00000475991.2:n.765+169_765+170insTC
ENST00000545985.5:c.984+169_984+170insTC	ENSP00000475241.2:n.984+169_984+170insTC
NM_001164277.1:c.984+169_984+170insTC , LRG_187t1:c.984+169_984+170insTC	NP_001157749.1:n.984+169_984+170insTC
NM_001164278.1:c.985-41_985-40insTC	NP_001157750.1:n.985-41_985-40insTC
NM_001164279.1:c.765+169_765+170insTC	NP_001157751.1:n.765+169_765+170insTC
NM_001164280.1:c.984+169_984+170insTC	NP_001157752.1:n.984+169_984+170insTC
NM_001467.5:c.984+169_984+170insTC	NP_001458.1:n.984+169_984+170insTC
NM_001164278.2:c.985-41_985-40insTC	NP_001157750.1:n.985-41_985-40insTC
NM_001164279.2:c.765+169_765+170insTC	NP_001157751.1:n.765+169_765+170insTC
NM_001164280.2:c.984+169_984+170insTC	NP_001157752.1:n.984+169_984+170insTC
NM_001467.6:c.984+169_984+170insTC	NP_001458.1:n.984+169_984+170insTC
NM_001164277.2:c.984+169_984+170insTC MANE Select	NP_001157749.1:n.984+169_984+170insTC