Canonical Allele Identifier: CA3327458

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654889_80654897del , CM000667.2:g.80654889_80654897del	GRCh38
NC_000005.9:g.79950708_79950716del , CM000667.1:g.79950708_79950716del	GRCh37
NC_000005.8:g.79986464_79986472del	NCBI36
NG_016607.1:g.5415_5423del
NG_023304.1:g.5096_5104del
NG_016607.2:g.5415_5423del

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-397_-389del (DHFR) MANE Select	NP_000782.1:n.-397_-389del
NM_002439.5:c.162_170del (MSH3) MANE Select	NP_002430.3:p.Ala55_Ala57del
ENST00000265081.7:c.162_170del (MSH3) MANE Select	ENSP00000265081.6:p.Ala55_Ala57del
ENST00000439211.7:c.-397_-389del (DHFR) MANE Select	ENSP00000396308.2:n.-397_-389del
NM_000791.3:c.-397_-389del (DHFR)	NP_000782.1:n.-397_-389del
NM_001290354.1:c.-503_-495del (DHFR)	NP_001277283.1:n.-503_-495del
NM_001290354.2:c.-503_-495del (DHFR)	NP_001277283.1:n.-503_-495del
NM_001290357.1:c.-397_-389del (DHFR)	NP_001277286.1:n.-397_-389del
NM_001290357.2:c.-397_-389del (DHFR)	NP_001277286.1:n.-397_-389del
NM_002439.4:c.162_170del (MSH3)	NP_002430.3:p.Ala55_Ala57del
NR_110936.1:n.96_104del (DHFR)
NR_110936.2:n.98_106del (DHFR)
ENST00000265081.6:c.162_170del (MSH3)	ENSP00000265081.6:p.Ala55_Ala57del
ENST00000439211.6:c.-397_-389del (DHFR)	ENSP00000396308.2:n.-397_-389del
ENST00000667069.1:c.162_170del (MSH3)	ENSP00000499502.1:p.Ala55_Ala57del
ENST00000670357.1:c.162_170del (MSH3)	ENSP00000499791.1:p.Ala55_Ala57del