Canonical Allele Identifier: CA1163306441

Gene: MTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.37812898_37812909delinsACCTCCTGCCTT , CM000663.2:g.37812898_37812909delinsACCTCCTGCCTT	GRCh38
NC_000001.10:g.38278570_38278581delinsACCTCCTGCCTT , CM000663.1:g.38278570_38278581delinsACCTCCTGCCTT	GRCh37
NC_000001.9:g.38051157_38051168delinsACCTCCTGCCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373036.5:c.*2227_*2238delinsAAGGCAGGAGGT MANE Select	ENSP00000362127.3:n.*2227_*2238delinsAAGGCAGGAGGT
ENST00000373036.4:c.*2227_*2238delinsAAGGCAGGAGGT	ENSP00000362127.3:n.*2227_*2238delinsAAGGCAGGAGGT
NM_005955.2:c.*2227_*2238delinsAAGGCAGGAGGT	NP_005946.2:n.*2227_*2238delinsAAGGCAGGAGGT
XM_011541491.1:c.*2227_*2238delinsAAGGCAGGAGGT	XP_011539793.1:n.*2227_*2238delinsAAGGCAGGAGGT
XM_011541492.1:c.*2227_*2238delinsAAGGCAGGAGGT	XP_011539794.1:n.*2227_*2238delinsAAGGCAGGAGGT
XM_011541494.1:c.*2227_*2238delinsAAGGCAGGAGGT	XP_011539796.1:n.*2227_*2238delinsAAGGCAGGAGGT
XM_011541491.2:c.*2227_*2238delinsAAGGCAGGAGGT	XP_011539793.1:n.*2227_*2238delinsAAGGCAGGAGGT
NM_005955.3:c.*2227_*2238delinsAAGGCAGGAGGT MANE Select	NP_005946.2:n.*2227_*2238delinsAAGGCAGGAGGT