Canonical Allele Identifier: CA2984202535

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654892_80654906del , CM000667.2:g.80654892_80654906del	GRCh38
NC_000005.9:g.79950711_79950725del , CM000667.1:g.79950711_79950725del	GRCh37
NC_000005.8:g.79986467_79986481del	NCBI36
NG_016607.1:g.5418_5432del
NG_023304.1:g.5078_5092del
NG_016607.2:g.5418_5432del

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-415_-401del (DHFR) MANE Select	NP_000782.1:n.-415_-401del
NM_002439.5:c.165_179del (MSH3) MANE Select	NP_002430.3:p.Ala56_Ala60del
ENST00000265081.7:c.165_179del (MSH3) MANE Select	ENSP00000265081.6:p.Ala56_Ala60del
ENST00000439211.7:c.-415_-401del (DHFR) MANE Select	ENSP00000396308.2:n.-415_-401del
NM_000791.3:c.-415_-401del (DHFR)	NP_000782.1:n.-415_-401del
NM_001290354.1:c.-521_-507del (DHFR)	NP_001277283.1:n.-521_-507del
NM_001290354.2:c.-521_-507del (DHFR)	NP_001277283.1:n.-521_-507del
NM_001290357.1:c.-415_-401del (DHFR)	NP_001277286.1:n.-415_-401del
NM_001290357.2:c.-415_-401del (DHFR)	NP_001277286.1:n.-415_-401del
NM_002439.4:c.165_179del (MSH3)	NP_002430.3:p.Ala56_Ala60del
NR_110936.1:n.78_92del (DHFR)
NR_110936.2:n.80_94del (DHFR)
ENST00000265081.6:c.165_179del (MSH3)	ENSP00000265081.6:p.Ala56_Ala60del
ENST00000439211.6:c.-415_-401del (DHFR)	ENSP00000396308.2:n.-415_-401del
ENST00000667069.1:c.165_179del (MSH3)	ENSP00000499502.1:p.Ala56_Ala60del
ENST00000670357.1:c.165_179del (MSH3)	ENSP00000499791.1:p.Ala56_Ala60del