Canonical Allele Identifier: CA560769285

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654926_80654934dup , CM000667.2:g.80654926_80654934dup	GRCh38
NC_000005.9:g.79950745_79950753dup , CM000667.1:g.79950745_79950753dup	GRCh37
NC_000005.8:g.79986501_79986509dup	NCBI36
NG_016607.1:g.5452_5460dup
NG_023304.1:g.5051_5059dup
NG_016607.2:g.5452_5460dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.199_207dup (MSH3) MANE Select	ENSP00000265081.6:p.Pro69_Ala70insProAlaPro
ENST00000439211.7:c.-442_-434dup (DHFR) MANE Select	ENSP00000396308.2:n.-442_-434dup
ENST00000667069.1:c.199_207dup (MSH3)	ENSP00000499502.1:p.Pro69_Ala70insProAlaPro
ENST00000670357.1:c.199_207dup (MSH3)	ENSP00000499791.1:p.Pro69_Ala70insProAlaPro
ENST00000265081.6:c.199_207dup (MSH3)	ENSP00000265081.6:p.Pro69_Ala70insProAlaPro
ENST00000439211.6:c.-442_-434dup (DHFR)	ENSP00000396308.2:n.-442_-434dup
NM_000791.3:c.-442_-434dup (DHFR)	NP_000782.1:n.-442_-434dup
NM_001290354.1:c.-548_-540dup (DHFR)	NP_001277283.1:n.-548_-540dup
NM_001290357.1:c.-442_-434dup (DHFR)	NP_001277286.1:n.-442_-434dup
NM_002439.4:c.199_207dup (MSH3)	NP_002430.3:p.Pro69_Ala70insProAlaPro
NR_110936.1:n.51_59dup (DHFR)
NM_000791.4:c.-442_-434dup (DHFR) MANE Select	NP_000782.1:n.-442_-434dup
NM_002439.5:c.199_207dup (MSH3) MANE Select	NP_002430.3:p.Pro69_Ala70insProAlaPro
NM_001290354.2:c.-548_-540dup (DHFR)	NP_001277283.1:n.-548_-540dup
NM_001290357.2:c.-442_-434dup (DHFR)	NP_001277286.1:n.-442_-434dup
NR_110936.2:n.53_61dup (DHFR)