Canonical Allele Identifier: CA2674438758

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628877-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628877_80628878insCC , CM000667.2:g.80628877_80628878insCC	GRCh38
NC_000005.9:g.79924696_79924697insCC , CM000667.1:g.79924696_79924697insCC	GRCh37
NC_000005.8:g.79960452_79960453insCC	NCBI36
NG_023304.1:g.31104_31105insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*209_*210insGG MANE Select	ENSP00000396308.2:n.*209_*210insGG
ENST00000439211.6:c.*209_*210insGG	ENSP00000396308.2:n.*209_*210insGG
ENST00000504396.1:c.*209_*210insGG	ENSP00000421334.1:n.*209_*210insGG
ENST00000505337.5:c.*109_*110insGG	ENSP00000426474.1:n.*109_*110insGG
ENST00000511032.5:c.*267_*268insGG	ENSP00000422732.1:n.*267_*268insGG
ENST00000513048.5:n.654_655insGG
NM_000791.3:c.*209_*210insGG	NP_000782.1:n.*209_*210insGG
NM_001290354.1:c.*209_*210insGG	NP_001277283.1:n.*209_*210insGG
NM_001290357.1:c.*267_*268insGG	NP_001277286.1:n.*267_*268insGG
NR_110936.1:n.1088_1089insGG
NM_000791.4:c.*209_*210insGG MANE Select	NP_000782.1:n.*209_*210insGG
NM_001290354.2:c.*209_*210insGG	NP_001277283.1:n.*209_*210insGG
NM_001290357.2:c.*267_*268insGG	NP_001277286.1:n.*267_*268insGG
NR_110936.2:n.1090_1091insGG