Canonical Allele Identifier: CA2003775860

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029776_119029777delinsCA , CM000673.2:g.119029776_119029777delinsCA	GRCh38
NC_000011.9:g.118900486_118900487delinsCA , CM000673.1:g.118900486_118900487delinsCA	GRCh37
NC_000011.8:g.118405696_118405697delinsCA	NCBI36
NG_013331.1:g.6130_6131delinsTG , LRG_187:g.6130_6131delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-213_35-212delinsTG
ENST00000697846.1:n.35-213_35-212delinsTG
ENST00000697847.1:n.35-213_35-212delinsTG
ENST00000697848.1:n.35-213_35-212delinsTG
ENST00000697849.1:n.66_67delinsTG
ENST00000697850.1:n.35-213_35-212delinsTG
ENST00000697851.1:n.66_67delinsTG
ENST00000638186.1:n.108+90_108+91delinsTG
ENST00000638360.1:n.43-213_43-212delinsTG
ENST00000638925.1:n.42-213_42-212delinsTG
ENST00000650539.1:n.211-213_211-212delinsTG
ENST00000330775.9:c.-195-213_-195-212delinsTG	ENSP00000476242.2:n.-195-213_-195-212delinsTG
ENST00000357590.9:c.-195-213_-195-212delinsTG	ENSP00000476176.2:n.-195-213_-195-212delinsTG
ENST00000525039.5:n.229-213_229-212delinsTG
ENST00000525102.5:n.563-213_563-212delinsTG
ENST00000527992.5:n.33-213_33-212delinsTG
ENST00000530407.5:n.25-213_25-212delinsTG
ENST00000532085.1:n.1087_1088delinsTG
ENST00000534384.1:n.25+139_25+140delinsTG
ENST00000538950.5:c.-344-213_-344-212delinsTG	ENSP00000475991.2:n.-344-213_-344-212delinsTG
ENST00000545985.5:c.-195-213_-195-212delinsTG	ENSP00000475241.2:n.-195-213_-195-212delinsTG
NM_001164277.1:c.-195-213_-195-212delinsTG , LRG_187t1:c.-195-213_-195-212delinsTG	NP_001157749.1:n.-195-213_-195-212delinsTG
NM_001164278.1:c.-195-213_-195-212delinsTG	NP_001157750.1:n.-195-213_-195-212delinsTG
NM_001164279.1:c.-344-213_-344-212delinsTG	NP_001157751.1:n.-344-213_-344-212delinsTG
NM_001467.5:c.-195-213_-195-212delinsTG	NP_001458.1:n.-195-213_-195-212delinsTG
NM_001164278.2:c.-195-213_-195-212delinsTG	NP_001157750.1:n.-195-213_-195-212delinsTG
NM_001164279.2:c.-344-213_-344-212delinsTG	NP_001157751.1:n.-344-213_-344-212delinsTG
NM_001467.6:c.-195-213_-195-212delinsTG	NP_001458.1:n.-195-213_-195-212delinsTG
NM_001164277.2:c.-195-213_-195-212delinsTG MANE Select	NP_001157749.1:n.-195-213_-195-212delinsTG