Canonical Allele Identifier: CA2674441055
Community Standard Title: NM_000791.4(DHFR):c.-426_-388dup

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80654878_80654916dup , CM000667.2:g.80654878_80654916dup GRCh38
NC_000005.9:g.79950697_79950735dup , CM000667.1:g.79950697_79950735dup GRCh37
NC_000005.8:g.79986453_79986491dup NCBI36
NG_016607.1:g.5404_5442dup
NG_023304.1:g.5067_5105dup
NG_016607.2:g.5404_5442dup

Transcript Alleles

HGVS Amino-acid Change
NM_000791.4:c.-426_-388dup (DHFR) MANE Select NP_000782.1:n.-426_-388dup
NM_002439.5:c.151_189dup (MSH3) MANE Select NP_002430.3:p.Pro63_Pro64insAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAla...
ENST00000265081.7:c.151_189dup (MSH3) MANE Select ENSP00000265081.6:p.Pro63_Pro64insAlaAlaAlaAlaAlaAlaAlaAlaAla...
ENST00000439211.7:c.-426_-388dup (DHFR) MANE Select ENSP00000396308.2:n.-426_-388dup
NM_000791.3:c.-426_-388dup (DHFR) NP_000782.1:n.-426_-388dup
NM_001290354.1:c.-532_-494dup (DHFR) NP_001277283.1:n.-532_-494dup
NM_001290354.2:c.-532_-494dup (DHFR) NP_001277283.1:n.-532_-494dup
NM_001290357.1:c.-426_-388dup (DHFR) NP_001277286.1:n.-426_-388dup
NM_001290357.2:c.-426_-388dup (DHFR) NP_001277286.1:n.-426_-388dup
NM_002439.4:c.151_189dup (MSH3) NP_002430.3:p.Pro63_Pro64insAlaAlaAlaAlaAlaAlaAlaAlaAlaAlaAla...
NR_110936.1:n.67_105dup (DHFR)
NR_110936.2:n.69_107dup (DHFR)
ENST00000265081.6:c.151_189dup (MSH3) ENSP00000265081.6:p.Pro63_Pro64insAlaAlaAlaAlaAlaAlaAlaAlaAla...
ENST00000439211.6:c.-426_-388dup (DHFR) ENSP00000396308.2:n.-426_-388dup
ENST00000667069.1:c.151_189dup (MSH3) ENSP00000499502.1:p.Pro63_Pro64insAlaAlaAlaAlaAlaAlaAlaAlaAla...
ENST00000670357.1:c.151_189dup (MSH3) ENSP00000499791.1:p.Pro63_Pro64insAlaAlaAlaAlaAlaAlaAlaAlaAla...