Canonical Allele Identifier: CA3327474

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654896_80654913del , CM000667.2:g.80654896_80654913del	GRCh38
NC_000005.9:g.79950715_79950732del , CM000667.1:g.79950715_79950732del	GRCh37
NC_000005.8:g.79986471_79986488del	NCBI36
NG_016607.1:g.5422_5439del
NG_023304.1:g.5075_5092del
NG_016607.2:g.5422_5439del

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-418_-401del (DHFR) MANE Select	NP_000782.1:n.-418_-401del
NM_002439.5:c.169_186del (MSH3) MANE Select	NP_002430.3:p.Ala57_Ala62del
ENST00000265081.7:c.169_186del (MSH3) MANE Select	ENSP00000265081.6:p.Ala57_Ala62del
ENST00000439211.7:c.-418_-401del (DHFR) MANE Select	ENSP00000396308.2:n.-418_-401del
NM_000791.3:c.-418_-401del (DHFR)	NP_000782.1:n.-418_-401del
NM_001290354.1:c.-524_-507del (DHFR)	NP_001277283.1:n.-524_-507del
NM_001290354.2:c.-524_-507del (DHFR)	NP_001277283.1:n.-524_-507del
NM_001290357.1:c.-418_-401del (DHFR)	NP_001277286.1:n.-418_-401del
NM_001290357.2:c.-418_-401del (DHFR)	NP_001277286.1:n.-418_-401del
NM_002439.4:c.169_186del (MSH3)	NP_002430.3:p.Ala57_Ala62del
NR_110936.1:n.75_92del (DHFR)
NR_110936.2:n.77_94del (DHFR)
ENST00000265081.6:c.169_186del (MSH3)	ENSP00000265081.6:p.Ala57_Ala62del
ENST00000439211.6:c.-418_-401del (DHFR)	ENSP00000396308.2:n.-418_-401del
ENST00000667069.1:c.169_186del (MSH3)	ENSP00000499502.1:p.Ala57_Ala62del
ENST00000670357.1:c.169_186del (MSH3)	ENSP00000499791.1:p.Ala57_Ala62del