Canonical Allele Identifier: CA170987

Gene: DHFR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654344_80654345insTGGCGCGTCCCGCCCAGGT , CM000667.2:g.80654344_80654345insTGGCGCGTCCCGCCCAGGT	GRCh38
NC_000005.9:g.79950163_79950164insTGGCGCGTCCCGCCCAGGT , CM000667.1:g.79950163_79950164insTGGCGCGTCCCGCCCAGGT	GRCh37
NC_000005.8:g.79985919_79985920insTGGCGCGTCCCGCCCAGGT	NCBI36
NG_016607.1:g.4870_4871insTGGCGCGTCCCGCCCAGGT
NG_023304.1:g.5637_5638insACCTGGGCGGGACGCGCCA
NG_016607.2:g.4870_4871insTGGCGCGTCCCGCCCAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.86+59_86+60insACCTGGGCGGGACGCGCCA MANE Select	ENSP00000396308.2:n.86+59_86+60insACCTGGGCGGGACGCGCCA
ENST00000439211.6:c.86+59_86+60insACCTGGGCGGGACGCGCCA	ENSP00000396308.2:n.86+59_86+60insACCTGGGCGGGACGCGCCA
ENST00000504396.1:c.-21+59_-21+60insACCTGGGCGGGACGCGCCA	ENSP00000421334.1:n.-21+59_-21+60insACCTGGGCGGGACGCGCCA
ENST00000505337.5:c.86+59_86+60insACCTGGGCGGGACGCGCCA	ENSP00000426474.1:n.86+59_86+60insACCTGGGCGGGACGCGCCA
ENST00000511032.5:c.86+59_86+60insACCTGGGCGGGACGCGCCA	ENSP00000422732.1:n.86+59_86+60insACCTGGGCGGGACGCGCCA
ENST00000513048.5:n.144+59_144+60insACCTGGGCGGGACGCGCCA
NM_000791.3:c.86+59_86+60insACCTGGGCGGGACGCGCCA	NP_000782.1:n.86+59_86+60insACCTGGGCGGGACGCGCCA
NM_001290354.1:c.-21+59_-21+60insACCTGGGCGGGACGCGCCA	NP_001277283.1:n.-21+59_-21+60insACCTGGGCGGGACGCGCCA
NM_001290357.1:c.86+59_86+60insACCTGGGCGGGACGCGCCA	NP_001277286.1:n.86+59_86+60insACCTGGGCGGGACGCGCCA
NR_110936.1:n.578+59_578+60insACCTGGGCGGGACGCGCCA
NM_000791.4:c.86+59_86+60insACCTGGGCGGGACGCGCCA MANE Select	NP_000782.1:n.86+59_86+60insACCTGGGCGGGACGCGCCA
NM_001290354.2:c.-21+59_-21+60insACCTGGGCGGGACGCGCCA	NP_001277283.1:n.-21+59_-21+60insACCTGGGCGGGACGCGCCA
NM_001290357.2:c.86+59_86+60insACCTGGGCGGGACGCGCCA	NP_001277286.1:n.86+59_86+60insACCTGGGCGGGACGCGCCA
NR_110936.2:n.580+59_580+60insACCTGGGCGGGACGCGCCA